{
    "disease_id": "DOID:0050736",
    "recommended_name": {
        "id": "DOID:0050736",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050736",
        "name": "autosomal dominant disease",
        "description": "An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease."
    },
    "synonyms": [],
    "children": [
        {
            "id": "DOID:0050156",
            "label": "idiopathic pulmonary fibrosis",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050331",
            "label": "lacrimoauriculodentodigital syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050429",
            "label": "Hailey-Hailey disease",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050430",
            "label": "multiple endocrine neoplasia type 2A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050434",
            "label": "Andersen-Tawil syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050438",
            "label": "Frasier syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050449",
            "label": "pachyonychia congenita",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050463",
            "label": "campomelic dysplasia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050466",
            "label": "Loeys-Dietz syndrome",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0060964",
                    "label": "Loeys-Dietz syndrome 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070233",
                    "label": "Loeys-Dietz syndrome 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070234",
                    "label": "Loeys-Dietz syndrome 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070235",
                    "label": "Loeys-Dietz syndrome 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070236",
                    "label": "Loeys-Dietz syndrome 5",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070237",
                    "label": "Loeys-Dietz syndrome 3",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050469",
            "label": "Costello syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050471",
            "label": "Carney complex",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050472",
            "label": "monilethrix",
            "link_status": false,
            "children": [
                {
                    "id": "DOID:0061145",
                    "label": "monilethrix 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061152",
                    "label": "monilethrix 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061153",
                    "label": "monilethrix 3",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050524",
            "label": "maturity-onset diabetes of the young",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0111099",
                    "label": "maturity-onset diabetes of the young type 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111100",
                    "label": "maturity-onset diabetes of the young type 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111102",
                    "label": "maturity-onset diabetes of the young type 3",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111103",
                    "label": "maturity-onset diabetes of the young type 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111104",
                    "label": "maturity-onset diabetes of the young type 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111105",
                    "label": "maturity-onset diabetes of the young type 8",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111106",
                    "label": "maturity-onset diabetes of the young type 7",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111107",
                    "label": "maturity-onset diabetes of the young type 9",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111108",
                    "label": "maturity-onset diabetes of the young type 10",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111109",
                    "label": "maturity-onset diabetes of the young type 11",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111110",
                    "label": "maturity-onset diabetes of the young type 13",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111111",
                    "label": "maturity-onset diabetes of the young type 14",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050540",
            "label": "Charcot-Marie-Tooth disease type 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050546",
            "label": "congenital adrenal insufficiency",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050547",
            "label": "familial medullary thyroid carcinoma",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050558",
            "label": "Ullrich congenital muscular dystrophy",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0060942",
                    "label": "Ullrich congenital muscular dystrophy 1B",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0060943",
                    "label": "Ullrich congenital muscular dystrophy 1C",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0060946",
                    "label": "Ullrich congenital muscular dystrophy 1A",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0060948",
                    "label": "Ullrich congenital muscular dystrophy 2",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050564",
            "label": "autosomal dominant nonsyndromic deafness",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0060690",
                    "label": "autosomal dominant auditory neuropathy 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070601",
                    "label": "autosomal dominant nonsyndromic deafness 37",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070602",
                    "label": "autosomal dominant nonsyndromic deafness 80",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070603",
                    "label": "autosomal dominant nonsyndromic deafness 82",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070604",
                    "label": "autosomal dominant nonsyndromic deafness 84",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070605",
                    "label": "autosomal dominant nonsyndromic deafness 85",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070606",
                    "label": "autosomal dominant nonsyndromic deafness 87",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070607",
                    "label": "autosomal dominant nonsyndromic deafness 90",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070608",
                    "label": "autosomal dominant nonsyndromic deafness 81",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070609",
                    "label": "autosomal dominant nonsyndromic deafness 83",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070610",
                    "label": "autosomal dominant nonsyndromic deafness 86",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070611",
                    "label": "autosomal dominant nonsyndromic deafness 88",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070612",
                    "label": "autosomal dominant nonsyndromic deafness 89",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080267",
                    "label": "autosomal dominant nonsyndromic deafness 71",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080268",
                    "label": "autosomal dominant nonsyndromic deafness 72",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080269",
                    "label": "autosomal dominant nonsyndromic deafness 73",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080270",
                    "label": "autosomal dominant nonsyndromic deafness 34",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110541",
                    "label": "autosomal dominant nonsyndromic deafness 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110542",
                    "label": "autosomal dominant nonsyndromic deafness 10",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110543",
                    "label": "autosomal dominant nonsyndromic deafness 11",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110544",
                    "label": "autosomal dominant nonsyndromic deafness 12",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110545",
                    "label": "autosomal dominant nonsyndromic deafness 13",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110546",
                    "label": "autosomal dominant nonsyndromic deafness 15",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110548",
                    "label": "autosomal dominant nonsyndromic deafness 17",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110550",
                    "label": "autosomal dominant nonsyndromic deafness 20",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110551",
                    "label": "autosomal dominant nonsyndromic deafness 21",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110552",
                    "label": "autosomal dominant nonsyndromic deafness 22",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110553",
                    "label": "autosomal dominant nonsyndromic deafness 23",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110555",
                    "label": "autosomal dominant nonsyndromic deafness 25",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110556",
                    "label": "autosomal dominant nonsyndromic deafness 27",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110557",
                    "label": "autosomal dominant nonsyndromic deafness 28",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110558",
                    "label": "autosomal dominant nonsyndromic deafness 2A",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110559",
                    "label": "autosomal dominant nonsyndromic deafness 2B",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110563",
                    "label": "autosomal dominant nonsyndromic deafness 36",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110564",
                    "label": "autosomal dominant nonsyndromic deafness 3A",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110565",
                    "label": "autosomal dominant nonsyndromic deafness 3B",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110566",
                    "label": "autosomal dominant nonsyndromic deafness 40",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110567",
                    "label": "autosomal dominant nonsyndromic deafness 41",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110569",
                    "label": "autosomal dominant nonsyndromic deafness 44",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110573",
                    "label": "autosomal dominant nonsyndromic deafness 4A",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110574",
                    "label": "autosomal dominant nonsyndromic deafness 4B",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110575",
                    "label": "autosomal dominant nonsyndromic deafness 5",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110581",
                    "label": "autosomal dominant nonsyndromic deafness 56",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110584",
                    "label": "autosomal dominant nonsyndromic deafness 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110585",
                    "label": "autosomal dominant nonsyndromic deafness 64",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110586",
                    "label": "autosomal dominant nonsyndromic deafness 65",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110587",
                    "label": "autosomal dominant nonsyndromic deafness 66",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110588",
                    "label": "autosomal dominant nonsyndromic deafness 67",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110589",
                    "label": "autosomal dominant nonsyndromic deafness 68",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110590",
                    "label": "autosomal dominant nonsyndromic deafness 69",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110591",
                    "label": "autosomal dominant nonsyndromic deafness 7",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110592",
                    "label": "autosomal dominant nonsyndromic deafness 70",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110593",
                    "label": "autosomal dominant nonsyndromic deafness 9",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0112159",
                    "label": "autosomal dominant nonsyndromic deafness 78",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0112160",
                    "label": "autosomal dominant nonsyndromic deafness 79",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0112165",
                    "label": "autosomal dominant nonsyndromic deafness 74",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0112166",
                    "label": "autosomal dominant nonsyndromic deafness 75",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0112167",
                    "label": "autosomal dominant nonsyndromic deafness 76",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0112168",
                    "label": "autosomal dominant nonsyndromic deafness 77",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0112373",
                    "label": "autosomal dominant auditory neuropathy 3",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050601",
            "label": "ADULT syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050606",
            "label": "acrokeratosis verruciformis",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050628",
            "label": "advanced sleep phase syndrome",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0061006",
                    "label": "advanced sleep phase syndrome 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110011",
                    "label": "advanced sleep phase syndrome 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110012",
                    "label": "advanced sleep phase syndrome 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110013",
                    "label": "advanced sleep phase syndrome 3",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050636",
            "label": "hereditary systemic amyloidosis 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050637",
            "label": "Finnish type amyloidosis",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050638",
            "label": "hereditary systemic amyloidosis 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050657",
            "label": "Cowden syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050658",
            "label": "Bart-Pumphrey syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050660",
            "label": "Beare-Stevenson cutis gyrata syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050675",
            "label": "Birk-Barel syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050676",
            "label": "Birt-Hogg-Dube syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050678",
            "label": "Blau syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050689",
            "label": "brachydactyly-syndactyly syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050691",
            "label": "branchiooculofacial syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050693",
            "label": "Brooke-Spiegler syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050770",
            "label": "polycystic liver disease",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0060975",
                    "label": "polycystic liver disease 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0060976",
                    "label": "polycystic liver disease 3",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0060977",
                    "label": "polycystic liver disease 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0060980",
                    "label": "polycystic liver disease 1",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050772",
            "label": "spastic ataxia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050773",
            "label": "paraganglioma",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0061216",
                    "label": "pheochromocytoma/paraganglioma syndrome 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061217",
                    "label": "pheochromocytoma/paraganglioma syndrome 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061218",
                    "label": "pheochromocytoma/paraganglioma syndrome 3",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061219",
                    "label": "pheochromocytoma/paraganglioma syndrome 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061220",
                    "label": "pheochromocytoma/paraganglioma syndrome 5",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061221",
                    "label": "pheochromocytoma/paraganglioma syndrome 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061222",
                    "label": "pheochromocytoma/paraganglioma syndrome 7",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050787",
            "label": "juvenile polyposis syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050788",
            "label": "proximal symphalangism",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0080787",
                    "label": "proximal symphalangism 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080788",
                    "label": "proximal symphalangism 2",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0050789",
            "label": "tarsal-carpal coalition syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050792",
            "label": "multiple cutaneous and mucosal venous malformations",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050794",
            "label": "multiple synostoses syndrome",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0081317",
                    "label": "multiple synostoses syndrome 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081318",
                    "label": "multiple synostoses syndrome 2",
                    "link_status": true,
                    "children": []
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                {
                    "id": "DOID:0081319",
                    "label": "multiple synostoses syndrome 3",
                    "link_status": true,
                    "children": []
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                {
                    "id": "DOID:0081320",
                    "label": "multiple synostoses syndrome 4",
                    "link_status": true,
                    "children": []
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        },
        {
            "id": "DOID:0050831",
            "label": "familial encephalopathy with neuroserpin inclusion bodies",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050854",
            "label": "Muckle-Wells syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050880",
            "label": "Koolen de Vries syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050887",
            "label": "Townes-Brocks syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0050948",
            "label": "autosomal dominant hypophosphatemic rickets",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051014",
            "label": "atypical autosomal dominant adult-onset demyelinating leukodystrophy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051017",
            "label": "visceral heterotaxy 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051043",
            "label": "Charcot-Marie-Tooth disease axonal type 2JJ",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051045",
            "label": "myofibrillar myopathy 13 with rimmed vacuoles",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051051",
            "label": "congenital disorder of glycosylation type IIw",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051067",
            "label": "Fontaine progeroid syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0051084",
            "label": "developmental and epileptic encephalopathy 112",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051086",
            "label": "developmental and epileptic encephalopathy 114",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0051089",
            "label": "developmental and epileptic encephalopathy 120",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060055",
            "label": "popliteal pterygium syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060062",
            "label": "autosomal dominant tubulointerstitial kidney disease",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0061118",
                    "label": "autosomal dominant tubulointerstitial kidney disease 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061119",
                    "label": "autosomal dominant tubulointerstitial kidney disease 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061120",
                    "label": "autosomal dominant tubulointerstitial kidney disease 5",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061121",
                    "label": "autosomal dominant tubulointerstitial kidney disease 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061122",
                    "label": "autosomal dominant tubulointerstitial kidney disease 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111101",
                    "label": "renal cysts and diabetes syndrome",
                    "link_status": true,
                    "children": []
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            ]
        },
        {
            "id": "DOID:0060173",
            "label": "Timothy syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060193",
            "label": "amyotrophic lateral sclerosis type 1",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0060255",
            "label": "rippling muscle disease 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0060307",
            "label": "autosomal dominant intellectual developmental disorder",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0051010",
                    "label": "Bryant-Li-Bhoj neurodevelopmental syndrome",
                    "link_status": true,
                    "children": [
                        {
                            "id": "DOID:0051011",
                            "label": "Bryant-Li-Bhoj neurodevelopmental syndrome 1",
                            "link_status": true,
                            "children": []
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                        {
                            "id": "DOID:0051012",
                            "label": "Bryant-Li-Bhoj neurodevelopmental syndrome 2",
                            "link_status": true,
                            "children": []
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                },
                {
                    "id": "DOID:0060933",
                    "label": "developmental delay, dysmorphic facies, and brain anomalies",
                    "link_status": true,
                    "children": []
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                {
                    "id": "DOID:0061031",
                    "label": "autosomal dominant intellectual developmental disorder 57",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061032",
                    "label": "autosomal dominant intellectual developmental disorder 58",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061033",
                    "label": "autosomal dominant intellectual developmental disorder 59",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061034",
                    "label": "autosomal dominant intellectual developmental disorder 61",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061035",
                    "label": "autosomal dominant intellectual developmental disorder 62",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061036",
                    "label": "autosomal dominant intellectual developmental disorder 63 with macrocephaly",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061037",
                    "label": "autosomal dominant intellectual developmental disorder 64",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061038",
                    "label": "autosomal dominant intellectual developmental disorder 65",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061039",
                    "label": "autosomal dominant intellectual developmental disorder 66",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061040",
                    "label": "autosomal dominant intellectual developmental disorder 67",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061041",
                    "label": "autosomal dominant intellectual developmental disorder 68",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061042",
                    "label": "autosomal dominant intellectual developmental disorder 69",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061043",
                    "label": "autosomal dominant intellectual developmental disorder 70",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061044",
                    "label": "autosomal dominant intellectual developmental disorder 71 with behavioral abnormalities",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061045",
                    "label": "autosomal dominant intellectual developmental disorder 72",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061046",
                    "label": "autosomal dominant intellectual developmental disorder 73",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061047",
                    "label": "autosomal dominant intellectual developmental disorder 74",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061048",
                    "label": "autosomal dominant intellectual developmental disorder 75",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061049",
                    "label": "autosomal dominant intellectual developmental disorder type FRA12A",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061050",
                    "label": "autosomal dominant intellectual developmental disorder 60 with seizures",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061129",
                    "label": "intellectual developmental disorder with dysmorphic facies and behavioral abnormalities",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061147",
                    "label": "neurodevelopmental disorder with or without autism or seizures",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061253",
                    "label": "neurodevelopmental disorder with speech delay, movement abnormalities, and seizures",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061254",
                    "label": "intellectual developmental disorder with seizures and dysmorphic facies",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070031",
                    "label": "autosomal dominant intellectual developmental disorder 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070032",
                    "label": "autosomal dominant intellectual developmental disorder 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070033",
                    "label": "autosomal dominant intellectual developmental disorder 3",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070035",
                    "label": "autosomal dominant intellectual developmental disorder 5",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070036",
                    "label": "autosomal dominant intellectual developmental disorder 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070037",
                    "label": "autosomal dominant intellectual developmental disorder 7",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070038",
                    "label": "autosomal dominant neurodevelopmental disorder with or without hyperkinetic movements and seizures",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070039",
                    "label": "NESCAV syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070040",
                    "label": "autosomal dominant intellectual developmental disorder 10",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070041",
                    "label": "autosomal dominant intellectual developmental disorder 11",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070043",
                    "label": "autosomal dominant intellectual developmental disorder 13",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070047",
                    "label": "Schuurs-Hoeijmakers Syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070048",
                    "label": "GAND syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070049",
                    "label": "autosomal dominant intellectual developmental disorder 19",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070050",
                    "label": "neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070051",
                    "label": "autosomal dominant intellectual developmental disorder 21",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070052",
                    "label": "autosomal dominant intellectual developmental disorder 22",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070053",
                    "label": "autosomal dominant intellectual developmental disorder 23",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070054",
                    "label": "Vulto-van Silfout-de Vries syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070055",
                    "label": "Xia-Gibbs Syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070056",
                    "label": "autosomal dominant intellectual developmental disorder 26",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070058",
                    "label": "Helsmoortel-Van Der Aa Syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070059",
                    "label": "autosomal dominant intellectual developmental disorder 29",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070060",
                    "label": "autosomal dominant intellectual developmental disorder 30",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070061",
                    "label": "autosomal dominant intellectual developmental disorder 31",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070062",
                    "label": "Arboleda-Tham syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070063",
                    "label": "autosomal dominant intellectual developmental disorder 33",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070064",
                    "label": "autosomal dominant intellectual developmental disorder 34",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070065",
                    "label": "autosomal dominant intellectual developmental disorder 35",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070066",
                    "label": "autosomal dominant intellectual developmental disorder 36",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070067",
                    "label": "White-Sutton syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070068",
                    "label": "autosomal dominant intellectual developmental disorder 38",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070069",
                    "label": "autosomal dominant intellectual developmental disorder 39",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070070",
                    "label": "autosomal dominant intellectual developmental disorder 40",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070071",
                    "label": "autosomal dominant intellectual developmental disorder 41",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070072",
                    "label": "autosomal dominant intellectual developmental disorder 42",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070073",
                    "label": "autosomal dominant intellectual developmental disorder 43",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070074",
                    "label": "autosomal dominant intellectual developmental disorder 44",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070416",
                    "label": "Luo-Schoch-Yamamoto syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070417",
                    "label": "neurodevelopmental disorder with speech impairment and dysmorphic facies",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070420",
                    "label": "developmental delay, hypotonia, and impaired language",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070469",
                    "label": "neurodevelopmental disorder with dysmorphic facies and thin corpus callosum",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070513",
                    "label": "neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070514",
                    "label": "neurodevelopmental disorder with dysmorphic facies and distal limb anomalies",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070529",
                    "label": "Sifrim-Hitz-Weiss syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070536",
                    "label": "neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070668",
                    "label": "Snijders Blok-Campeau syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070694",
                    "label": "neurodevelopmental disorder with congenital cardiac defects and variable renal and ocular abnormalities",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070709",
                    "label": "Popov-Chang syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070710",
                    "label": "neurodevelopmental disorder with speech delay and behavioral abnormalities",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070711",
                    "label": "Harel-Tora neurodevelopmental syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070713",
                    "label": "neurodevelopmental disorder with early-onset seizures, facial dysmorphism, and behavioral abnormalities",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070715",
                    "label": "Ramond-Elliott neurodevelopmental syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070717",
                    "label": "developmental delay with sleep apnea",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070747",
                    "label": "immunodeficiency, developmental delay, and hypohomocysteinemia",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070753",
                    "label": "neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070756",
                    "label": "neurodevelopmental disorder with variable motor and speech impairment",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070757",
                    "label": "Pilarowski-Bjornsson syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080226",
                    "label": "autosomal dominant intellectual developmental disorder 56",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080227",
                    "label": "autosomal dominant intellectual developmental disorder 55",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080228",
                    "label": "autosomal dominant intellectual developmental disorder 53",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080230",
                    "label": "autosomal dominant intellectual developmental disorder 54",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080231",
                    "label": "autosomal dominant intellectual developmental disorder 52",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080232",
                    "label": "autosomal dominant intellectual developmental disorder 51",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080233",
                    "label": "autosomal dominant intellectual developmental disorder 50",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080234",
                    "label": "Clark-Baraitser syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080235",
                    "label": "autosomal dominant intellectual developmental disorder 48",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080236",
                    "label": "autosomal dominant intellectual developmental disorder 45",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080237",
                    "label": "autosomal dominant intellectual developmental disorder 46",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080238",
                    "label": "autosomal dominant intellectual developmental disorder 47",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081262",
                    "label": "intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081275",
                    "label": "neurodevelopmental disorder with eye movement abnormalities and ataxia",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081362",
                    "label": "Pierpont syndrome",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081430",
                    "label": "intellectual developmental disorder with autistic features and language delay, with or without seizures",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111743",
                    "label": "cerebellar ataxia type 47",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:1925",
                    "label": "Coffin-Siris syndrome",
                    "link_status": true,
                    "children": [
                        {
                            "id": "DOID:0070042",
                            "label": "Coffin-Siris syndrome 1",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0070044",
                            "label": "Coffin-Siris syndrome 2",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0070045",
                            "label": "Coffin-Siris syndrome 3",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0070046",
                            "label": "Coffin-Siris syndrome 4",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0070057",
                            "label": "Coffin-Siris syndrome 9",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0080297",
                            "label": "Coffin-Siris syndrome 6",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0112367",
                            "label": "Coffin-Siris syndrome 8",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0112368",
                            "label": "Coffin-Siris syndrome 5",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0112369",
                            "label": "Coffin-Siris syndrome 7",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0112370",
                            "label": "Coffin-Siris syndrome 12",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0112371",
                            "label": "Coffin-Siris syndrome 10",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0112372",
                            "label": "Coffin-Siris syndrome 11",
                            "link_status": true,
                            "children": []
                        }
                    ]
                }
            ]
        },
        {
            "id": "DOID:0060330",
            "label": "Rapp-Hodgkin syndrome",
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            "id": "DOID:0060354",
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            "label": "Parkinson's disease 8",
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            "label": "chromosome 15q11.2 deletion syndrome",
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            "label": "chromosome 15q24 deletion syndrome",
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            "id": "DOID:0060404",
            "label": "chromosome 17q12 deletion syndrome",
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            "id": "DOID:0060409",
            "label": "NFIA-related disorder",
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            "id": "DOID:0060455",
            "label": "Thiel-Behnke corneal dystrophy",
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            "id": "DOID:0060456",
            "label": "Schnyder corneal dystrophy",
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            "id": "DOID:0060464",
            "label": "Feingold syndrome",
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            "id": "DOID:0060468",
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            "id": "DOID:0060475",
            "label": "myoclonic-atonic epilepsy",
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            "id": "DOID:0060485",
            "label": "Mowat-Wilson syndrome",
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            "id": "DOID:0060486",
            "label": "Perry syndrome",
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            "id": "DOID:0060488",
            "label": "Pitt-Hopkins syndrome",
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            "id": "DOID:0060550",
            "label": "ablepharon macrostomia syndrome",
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            "id": "DOID:0060578",
            "label": "Noonan syndrome 1",
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            "id": "DOID:0060581",
            "label": "Noonan syndrome 3",
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            "id": "DOID:0060582",
            "label": "Noonan syndrome 4",
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            "id": "DOID:0060583",
            "label": "Noonan syndrome 5",
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            "id": "DOID:0060584",
            "label": "Noonan syndrome 6",
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            "id": "DOID:0060585",
            "label": "Noonan syndrome 7",
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            "id": "DOID:0060586",
            "label": "Noonan syndrome 8",
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            "id": "DOID:0060587",
            "label": "Noonan syndrome 9",
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            "id": "DOID:0060588",
            "label": "Noonan syndrome 10",
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            "id": "DOID:0060591",
            "label": "WHIM syndrome 1",
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                    "id": "DOID:14221",
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            "id": "DOID:0060614",
            "label": "ulnar-mammary syndrome",
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            "label": "autosomal dominant nocturnal frontal lobe epilepsy",
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                    "id": "DOID:0060685",
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                    "id": "DOID:0060686",
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                    "id": "DOID:0060701",
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                    "id": "DOID:0060702",
                    "label": "familial hypocalciuric hypercalcemia 3",
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            "id": "DOID:0060703",
            "label": "Muenke Syndrome",
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            "id": "DOID:0060731",
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            "id": "DOID:0060739",
            "label": "hand-foot-genital syndrome",
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            "id": "DOID:0060745",
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            "id": "DOID:0060747",
            "label": "Duane-radial ray syndrome",
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            "label": "familial temporal lobe epilepsy 7",
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            "label": "familial temporal lobe epilepsy 8",
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            "label": "autosomal dominant Robinow syndrome 1",
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            "id": "DOID:0060782",
            "label": "EEC syndrome",
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            "id": "DOID:0060798",
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            "id": "DOID:0060838",
            "label": "isolated microphthalmia 7",
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            "id": "DOID:0060843",
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            "label": "autosomal dominant pseudohypoaldosteronism type 1",
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            "children": []
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            "id": "DOID:0060867",
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            "id": "DOID:0060871",
            "label": "autosomal dominant keratitis-ichthyosis-deafness syndrome",
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            "label": "dystonia 33",
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            "id": "DOID:0060941",
            "label": "interstitial lung disease 1",
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            "id": "DOID:0060945",
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            "id": "DOID:0060953",
            "label": "ZTTK syndrome",
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            "label": "Cornelia de Lange syndrome 6",
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            "label": "interstitial lung disease 2",
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            "id": "DOID:0060972",
            "label": "renal hypomagnesemia 7, with or without dilated cardiomyopathy",
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            "children": []
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            "id": "DOID:0060985",
            "label": "preaxial polydactyly type IV",
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            "children": []
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            "id": "DOID:0060986",
            "label": "preaxial polydactyly II",
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            "children": []
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            "id": "DOID:0060989",
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            "id": "DOID:0060992",
            "label": "bent bone dysplasia syndrome 1",
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            "id": "DOID:0060995",
            "label": "autosomal dominant isolated macrothrombocytopenia 2",
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            "children": []
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            "id": "DOID:0060996",
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            "children": []
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            "id": "DOID:0060998",
            "label": "striatal degeneration 2",
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            "children": []
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            "id": "DOID:0061008",
            "label": "craniosynostosis 6",
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            "children": []
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            "id": "DOID:0061009",
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            "id": "DOID:0061010",
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            "label": "craniosynostosis 3",
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            "id": "DOID:0061012",
            "label": "craniosynostosis 4",
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            "id": "DOID:0061017",
            "label": "combined pituitary hormone deficiency 4",
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            "children": []
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            "id": "DOID:0061018",
            "label": "combined or isolated pituitary hormone deficiency 8",
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            "children": []
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            "id": "DOID:0061019",
            "label": "combined or isolated pituitary hormone deficiency 1",
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            "id": "DOID:0061022",
            "label": "combined pituitary hormone deficiency 6",
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            "children": []
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            "id": "DOID:0061028",
            "label": "Duane retraction syndrome 2",
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            "children": []
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            "id": "DOID:0061029",
            "label": "Duane retraction syndrome 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061053",
            "label": "immunodeficiency 82",
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            "children": []
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            "id": "DOID:0061054",
            "label": "immunodeficiency 84",
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            "children": []
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            "id": "DOID:0061055",
            "label": "immunodeficiency 85",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061064",
            "label": "immunodeficiency 94",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061070",
            "label": "immunodeficiency 100",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061071",
            "label": "immunodeficiency 101",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061076",
            "label": "immunodeficiency 107",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061087",
            "label": "immunodeficiency 121",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061096",
            "label": "immunodeficiency 133",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061097",
            "label": "immunodeficiency 132B",
            "link_status": true,
            "children": []
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            "id": "DOID:0061100",
            "label": "autosomal dominant primary microcephaly",
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                    "id": "DOID:0051037",
                    "label": "autosomal dominant primary microcephaly 26",
                    "link_status": true,
                    "children": []
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                {
                    "id": "DOID:0051038",
                    "label": "autosomal dominant primary microcephaly 27",
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                    "children": []
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                {
                    "id": "DOID:0070295",
                    "label": "primary autosomal dominant microcephaly 18",
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                    "children": []
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        {
            "id": "DOID:0061101",
            "label": "immunodeficiency 132A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061104",
            "label": "retinitis pigmentosa 96",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061106",
            "label": "retinitis pigmentosa 91",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061108",
            "label": "retinitis pigmentosa 79",
            "link_status": true,
            "children": []
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            "id": "DOID:0061110",
            "label": "retinitis pigmentosa 97",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061125",
            "label": "immunodeficiency 131",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061144",
            "label": "complex cortical dysplasia with other brain malformations 13",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061146",
            "label": "Pan-Chung-Bellen syndrome",
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            "children": []
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            "id": "DOID:0061150",
            "label": "familial isolated hypoparathyroidism 1",
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            "children": []
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        {
            "id": "DOID:0061151",
            "label": "familial isolated hypoparathyroidism 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061156",
            "label": "CASGID syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061160",
            "label": "infantile onset multisystem autoimmune disease 1",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061169",
            "label": "autosomal dominant autoinflammation, panniculitis, and dermatosis syndrome",
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            "children": []
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            "id": "DOID:0061172",
            "label": "transient neonatal diabetes mellitus 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061174",
            "label": "transient neonatal diabetes mellitus 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061176",
            "label": "developmental and epileptic encephalopathy 118",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061179",
            "label": "Adams-Oliver syndrome 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061184",
            "label": "myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061185",
            "label": "autoinflammatory syndrome with cytopenia, hyperzincemia, and hypercalprotectinemia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0061187",
            "label": "multiple familial trichoepithelioma 1",
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            "children": []
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            "id": "DOID:0061189",
            "label": "neuronal ceroid lipofuscinosis 15",
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            "children": []
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            "id": "DOID:0061198",
            "label": "Bethlem myopathy 1A",
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            "children": []
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            "id": "DOID:0061199",
            "label": "Bethlem myopathy 1B",
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            "children": []
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            "id": "DOID:0061200",
            "label": "Bethlem myopathy 1C",
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            "children": []
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            "id": "DOID:0061201",
            "label": "Bethlem myopathy 2",
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            "id": "DOID:0061209",
            "label": "branchiootic syndrome 1",
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            "children": []
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            "id": "DOID:0061210",
            "label": "branchiootic syndrome 3",
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            "children": []
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            "id": "DOID:0061223",
            "label": "epidermolytic hyperkeratosis 2A",
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            "children": []
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            "id": "DOID:0061229",
            "label": "Camurati-Engelmann disease 1",
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            "children": []
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            "id": "DOID:0061230",
            "label": "Camurati-Engelmann disease 2",
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            "children": []
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            "id": "DOID:0061235",
            "label": "brain small vessel disease 5 with osteoporosis",
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            "children": []
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            "id": "DOID:0061236",
            "label": "brain small vessel disease 6 with leukoencephalopathy",
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            "children": []
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            "id": "DOID:0061246",
            "label": "periventricular nodular heterotopia 9",
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            "children": []
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            "id": "DOID:0061248",
            "label": "familial hyperaldosteronism III",
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            "children": []
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            "id": "DOID:0061249",
            "label": "familial hyperaldosteronism II",
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            "children": []
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            "id": "DOID:0061250",
            "label": "familial hyperaldosteronism IV",
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            "children": []
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            "id": "DOID:0061257",
            "label": "congenital myopathy 26",
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            "children": []
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        {
            "id": "DOID:0061269",
            "label": "periventricular nodular heterotopia 6",
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            "children": []
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        {
            "id": "DOID:0061270",
            "label": "periventricular nodular heterotopia 7",
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            "children": []
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            "id": "DOID:0061274",
            "label": "Weill-Marchesani syndrome 2",
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            "children": []
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            "id": "DOID:0070016",
            "label": "autosomal dominant dyskeratosis congenita 2",
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            "children": []
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            "id": "DOID:0070018",
            "label": "autosomal dominant dyskeratosis congenita 3",
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            "children": []
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        {
            "id": "DOID:0070023",
            "label": "autosomal dominant dyskeratosis congenita 6",
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            "children": []
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        {
            "id": "DOID:0070026",
            "label": "Revesz syndrome",
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            "children": []
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            "id": "DOID:0070027",
            "label": "CST3-related cerebral amyloid angiopathy",
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            "children": []
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            "id": "DOID:0070028",
            "label": "APP-related cerebral amyloid angiopathy",
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            "children": []
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            "id": "DOID:0070029",
            "label": "ITM2B-related cerebral amyloid angiopathy 1",
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            "children": []
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        {
            "id": "DOID:0070030",
            "label": "ITM2B-related cerebral amyloid angiopathy 2",
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            "children": []
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            "id": "DOID:0070080",
            "label": "schizophrenia 4",
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            "children": []
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            "id": "DOID:0070082",
            "label": "schizophrenia 6",
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            "children": []
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            "id": "DOID:0070091",
            "label": "schizophrenia 15",
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            "children": []
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            "id": "DOID:0070124",
            "label": "congenital nongoitrous hypothyroidism 2",
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            "children": []
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        {
            "id": "DOID:0070125",
            "label": "congenital nongoitrous hypothyroidism 5",
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            "children": []
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        {
            "id": "DOID:0070128",
            "label": "congenital nongoitrous hypothyroidism 6",
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            "children": []
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            "id": "DOID:0070142",
            "label": "autosomal dominant cutis laxa",
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                    "id": "DOID:0070130",
                    "label": "autosomal dominant cutis laxa 1",
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                    "children": []
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                    "id": "DOID:0070131",
                    "label": "autosomal dominant cutis laxa 3",
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                    "children": []
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                {
                    "id": "DOID:0070136",
                    "label": "autosomal dominant cutis laxa 2",
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                    "children": []
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            "id": "DOID:0070149",
            "label": "hereditary sensory and autonomic neuropathy type 7",
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            "children": []
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            "id": "DOID:0070162",
            "label": "hereditary sensory and autonomic neuropathy type 1",
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                    "id": "DOID:0070152",
                    "label": "hereditary sensory and autonomic neuropathy type 1A",
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                    "id": "DOID:0070154",
                    "label": "hereditary sensory neuropathy type 1F",
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                    "children": []
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                    "id": "DOID:0070156",
                    "label": "hereditary sensory neuropathy type 1D",
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                    "children": []
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                    "id": "DOID:0070157",
                    "label": "hereditary sensory and autonomic neuropathy type 1C",
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                    "children": []
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                    "id": "DOID:0070158",
                    "label": "hereditary sensory neuropathy type 1E",
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                    "children": []
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            "id": "DOID:0070164",
            "label": "spermatogenic failure 2",
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            "children": []
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            "id": "DOID:0070168",
            "label": "spermatogenic failure 3",
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            "children": []
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        {
            "id": "DOID:0070169",
            "label": "spermatogenic failure 8",
            "link_status": true,
            "children": []
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            "id": "DOID:0070171",
            "label": "spermatogenic failure 12",
            "link_status": true,
            "children": []
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            "id": "DOID:0070176",
            "label": "spermatogenic failure 4",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070178",
            "label": "spermatogenic failure 10",
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            "children": []
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        {
            "id": "DOID:0070180",
            "label": "spermatogenic failure 11",
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            "children": []
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            "id": "DOID:0070197",
            "label": "distal myopathy 1",
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            "children": []
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            "id": "DOID:0070202",
            "label": "familial partial lipodystrophy type 2",
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            "children": []
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            "id": "DOID:0070204",
            "label": "familial partial lipodystrophy type 3",
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            "children": []
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            "id": "DOID:0070205",
            "label": "familial partial lipodystrophy type 4",
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            "children": []
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            "id": "DOID:0070208",
            "label": "hereditary lymphedema IC",
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            "children": []
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            "id": "DOID:0070209",
            "label": "hereditary lymphedema ID",
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            "children": []
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            "id": "DOID:0070210",
            "label": "hereditary lymphedema IA",
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            "children": []
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            "id": "DOID:0070214",
            "label": "familial hyperinsulinemic hypoglycemia 7",
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            "children": []
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            "id": "DOID:0070216",
            "label": "familial hyperinsulinemic hypoglycemia 3",
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            "children": []
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            "id": "DOID:0070217",
            "label": "familial hyperinsulinemic hypoglycemia 6",
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            "children": []
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            "id": "DOID:0070218",
            "label": "familial hyperinsulinemic hypoglycemia 2",
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            "children": []
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            "id": "DOID:0070219",
            "label": "familial hyperinsulinemic hypoglycemia 1",
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            "children": []
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            "id": "DOID:0070220",
            "label": "familial hyperinsulinemic hypoglycemia 5",
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            "children": []
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            "id": "DOID:0070228",
            "label": "intrahepatic cholestasis of pregnancy 1",
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            "children": []
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            "id": "DOID:0070229",
            "label": "intrahepatic cholestasis of pregnancy 3",
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            "children": []
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            "id": "DOID:0070247",
            "label": "autosomal dominant Emery-Dreifuss muscular dystrophy 2",
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            "children": []
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            "id": "DOID:0070249",
            "label": "autosomal dominant Emery-Dreifuss muscular dystrophy 4",
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            "children": []
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            "id": "DOID:0070250",
            "label": "autosomal dominant Emery-Dreifuss muscular dystrophy 5",
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            "children": []
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            "id": "DOID:0070252",
            "label": "autosomal dominant Emery-Dreifuss muscular dystrophy 7",
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            "children": []
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            "id": "DOID:0070298",
            "label": "multiple epiphyseal dysplasia 2",
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            "children": []
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            "id": "DOID:0070299",
            "label": "multiple epiphyseal dysplasia 5",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070301",
            "label": "multiple epiphyseal dysplasia 6",
            "link_status": true,
            "children": []
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            "id": "DOID:0070303",
            "label": "multiple epiphyseal dysplasia 1",
            "link_status": true,
            "children": []
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            "id": "DOID:0070304",
            "label": "multiple epiphyseal dysplasia 3",
            "link_status": true,
            "children": []
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            "id": "DOID:0070316",
            "label": "Miura type epiphyseal chondrodysplasia",
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            "children": []
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        {
            "id": "DOID:0070337",
            "label": "epithelial recurrent erosion dystrophy",
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            "children": []
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            "id": "DOID:0070345",
            "label": "vertebral anomalies and variable endocrine and T-cell dysfunction",
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            "children": []
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        {
            "id": "DOID:0070348",
            "label": "spinal muscular atrophy with lower extremity predominant",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0070349",
                    "label": "spinal muscular atrophy with lower extremity predominant 2A",
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                    "children": []
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                    "id": "DOID:0070350",
                    "label": "spinal muscular atrophy with lower extremity predominant 2B",
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                    "children": []
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                {
                    "id": "DOID:0070351",
                    "label": "spinal muscular atrophy with lower extremity predominant 1",
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                    "children": []
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            "id": "DOID:0070353",
            "label": "cataract 47",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070365",
            "label": "nevoid basal cell carcinoma syndrome 1",
            "link_status": true,
            "children": []
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            "id": "DOID:0070375",
            "label": "developmental and epileptic encephalopathy 64",
            "link_status": true,
            "children": []
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            "id": "DOID:0070377",
            "label": "developmental and epileptic encephalopathy 96",
            "link_status": true,
            "children": []
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            "id": "DOID:0070378",
            "label": "developmental and epileptic encephalopathy 109",
            "link_status": true,
            "children": []
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            "id": "DOID:0070379",
            "label": "developmental and epileptic encephalopathy 6B",
            "link_status": true,
            "children": []
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            "id": "DOID:0070383",
            "label": "developmental and epileptic encephalopathy 97",
            "link_status": true,
            "children": []
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            "id": "DOID:0070384",
            "label": "developmental and epileptic encephalopathy 98",
            "link_status": true,
            "children": []
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            "id": "DOID:0070385",
            "label": "developmental and epileptic encephalopathy 99",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070386",
            "label": "developmental and epileptic encephalopathy 100",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070389",
            "label": "developmental and epileptic encephalopathy 103",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070390",
            "label": "developmental and epileptic encephalopathy 104",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070394",
            "label": "developmental and epileptic encephalopathy 108",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070400",
            "label": "hypomyelinating leukodystrophy 19",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070401",
            "label": "hypomyelinating leukodystrophy 25",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070402",
            "label": "hypomyelinating leukodystrophy 22",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070405",
            "label": "hypomyelinating leukodystrophy 16",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070406",
            "label": "hypomyelinating leukodystrophy 24",
            "link_status": true,
            "children": []
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            "id": "DOID:0070415",
            "label": "brachycephaly, trichomegaly, and developmental delay",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070418",
            "label": "vertebral hypersegmentation and orofacial anomalies",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070438",
            "label": "retinal macular dystrophy",
            "link_status": false,
            "children": [
                {
                    "id": "DOID:0070439",
                    "label": "North Carolina macular dystrophy",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070441",
                    "label": "retinal macular dystrophy 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070517",
                    "label": "retinal macular dystrophy 2",
                    "link_status": true,
                    "children": []
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        {
            "id": "DOID:0070442",
            "label": "paroxysmal nonkinesigenic dyskinesia 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070445",
            "label": "early-onset dystonia and/or spastic paraplegia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070455",
            "label": "hereditary spastic paraplegia 79A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070457",
            "label": "hereditary spastic paraplegia 88",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070459",
            "label": "hereditary spastic paraplegia 90A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070460",
            "label": "hereditary spastic paraplegia 90B",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070461",
            "label": "mitochondrial complex V (ATP synthase) deficiency nuclear type 4A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070466",
            "label": "carpal tunnel syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070467",
            "label": "carpal tunnel syndrome 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0070471",
            "label": "early-onset epilepsy 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070472",
            "label": "early-onset epilepsy 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070474",
            "label": "childhood-onset neurodegeneration with brain atrophy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070483",
            "label": "Watson syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070484",
            "label": "Legius syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070509",
            "label": "Schinzel Giedion syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070516",
            "label": "Mitchell syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070530",
            "label": "foveal hypoplasia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070532",
            "label": "aniridia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070533",
            "label": "long QT syndrome 16",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070545",
            "label": "developmental and epileptic encephalopathy 116",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070546",
            "label": "primary pigmented nodular adrenocortical disease 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070547",
            "label": "primary pigmented nodular adrenocortical disease 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070549",
            "label": "primary pigmented nodular adrenocortical disease 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070551",
            "label": "epidermolytic palmoplantar keratoderma 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070552",
            "label": "epidermolytic palmoplantar keratoderma 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070613",
            "label": "familial renal glucosuria",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070615",
            "label": "autoinflammation, antibody deficiency, and immune dysregulation syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070617",
            "label": "rhabdoid tumor predisposition syndrome",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0060997",
                    "label": "rhabdoid tumor predisposition syndrome 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0070618",
                    "label": "rhabdoid tumor predisposition syndrome 1",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0070636",
            "label": "mirror movements 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070637",
            "label": "mirror movements 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070638",
            "label": "mirror movements 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070640",
            "label": "hereditary spastic paraplegia 18A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070643",
            "label": "hereditary spastic paraplegia 91",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070647",
            "label": "hereditary spastic paraplegia 30A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070652",
            "label": "Nil-Deshwar neurodevelopmental syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070653",
            "label": "Fliedner-Zweier syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070657",
            "label": "congenital variant of Rett syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070666",
            "label": "infantile myofibromatosis 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070667",
            "label": "infantile myofibromatosis 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070679",
            "label": "congenital hypomyelinating neuropathy 2",
            "link_status": true,
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            "id": "DOID:0070685",
            "label": "congenital hydrocephalus 4",
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            "id": "DOID:0070687",
            "label": "normal pressure hydrocephalus 1",
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            "id": "DOID:0070705",
            "label": "dentin dysplasia type IB",
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            "id": "DOID:0070707",
            "label": "dentin dysplasia type II",
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            "id": "DOID:0070716",
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            "id": "DOID:0070722",
            "label": "adult-onset leukoencephalopathy without lacunae",
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            "id": "DOID:0070724",
            "label": "dental radicular dysplasia",
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            "id": "DOID:0070743",
            "label": "congenital facial palsy with ptosis and velopharyngeal dysfunction",
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            "id": "DOID:0080020",
            "label": "Jansen's metaphyseal chondrodysplasia",
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            "id": "DOID:0080028",
            "label": "spondyloepimetaphyseal dysplasia, Strudwick type",
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            "id": "DOID:0080030",
            "label": "spondyloepimetaphyseal dysplasia, Missouri type",
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            "id": "DOID:0080037",
            "label": "Worth syndrome",
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            "id": "DOID:0080041",
            "label": "hypochondroplasia",
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            "id": "DOID:0080045",
            "label": "Kniest dysplasia",
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            "id": "DOID:0080047",
            "label": "pseudoachondroplasia",
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            "id": "DOID:0080056",
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            "label": "nonsyndromic congenital nail disorder 3",
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            "label": "nonsyndromic congenital nail disorder 8",
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            "id": "DOID:0080089",
            "label": "tubular aggregate myopathy 1",
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            "id": "DOID:0080092",
            "label": "myofibrillar myopathy 1",
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            "id": "DOID:0080093",
            "label": "adult-onset myofibrillar myopathy 2A",
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            "id": "DOID:0080094",
            "label": "myofibrillar myopathy 3",
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            "id": "DOID:0080095",
            "label": "myofibrillar myopathy 4",
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            "id": "DOID:0080096",
            "label": "myofibrillar myopathy 5",
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            "id": "DOID:0080097",
            "label": "myofibrillar myopathy 6",
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            "id": "DOID:0080102",
            "label": "congenital myopathy 4A",
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            "id": "DOID:0080130",
            "label": "mitochondrial DNA depletion syndrome 12a",
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            "id": "DOID:0080137",
            "label": "multiple endocrine neoplasia type 4",
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            "id": "DOID:0080196",
            "label": "mandibulofacial dysostosis, Guion-Almeida type",
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            "id": "DOID:0080219",
            "label": "dystransthyretinemic hyperthyroxinemia",
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            "id": "DOID:0080243",
            "label": "amelogenesis imperfecta type 3B",
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            "id": "DOID:0080248",
            "label": "erythrokeratodermia variabilis et progressiva 2",
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            "id": "DOID:0080249",
            "label": "erythrokeratodermia variabilis et progressiva 3",
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            "id": "DOID:0080264",
            "label": "exudative vitreoretinopathy 7",
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            "children": []
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            "id": "DOID:0080280",
            "label": "gingival fibromatosis 5",
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            "children": []
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            "id": "DOID:0080282",
            "label": "developmental and epileptic encephalopathy 56",
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            "children": []
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            "id": "DOID:0080284",
            "label": "developmental and epileptic encephalopathy 57",
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            "children": []
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            "id": "DOID:0080285",
            "label": "developmental and epileptic encephalopathy 58",
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            "children": []
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            "id": "DOID:0080290",
            "label": "familial erythrocytosis 5",
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            "children": []
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            "id": "DOID:0080291",
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            "children": []
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            "id": "DOID:0080294",
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            "children": []
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            "id": "DOID:0080317",
            "label": "megalencephalic leukoencephalopathy with subcortical cysts 2B",
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            "children": []
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            "id": "DOID:0080328",
            "label": "Culler-Jones syndrome",
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            "id": "DOID:0080334",
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            "id": "DOID:0080338",
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            "id": "DOID:0080344",
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                    "id": "DOID:0080345",
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            "id": "DOID:0080376",
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            "id": "DOID:0080383",
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            "id": "DOID:0080409",
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            "id": "DOID:0080422",
            "label": "Dravet syndrome",
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            "id": "DOID:0080507",
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            "id": "DOID:0080508",
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            "id": "DOID:0080510",
            "label": "epidermolysis bullosa simplex 1C",
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            "id": "DOID:0080511",
            "label": "generalized intermediate epidermolysis bullosa simplex 1B",
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            "children": []
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            "id": "DOID:0080517",
            "label": "Meier-Gorlin syndrome 6",
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            "children": []
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            "id": "DOID:0080519",
            "label": "PAPA syndrome",
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            "children": []
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            "id": "DOID:0080523",
            "label": "adult-onset leukoencephalopathy with axonal spheroids and pigmented glia",
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            "id": "DOID:0080526",
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            "id": "DOID:0080527",
            "label": "bronchiectasis 2",
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            "id": "DOID:0080528",
            "label": "bronchiectasis 3",
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            "id": "DOID:0080533",
            "label": "Carney-Stratakis syndrome",
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            "children": []
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            "id": "DOID:0080538",
            "label": "Sweeney-Cox syndrome",
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            "children": []
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            "id": "DOID:0080584",
            "label": "autosomal dominant Wolfram syndrome",
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            "children": []
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            "id": "DOID:0080588",
            "label": "agammaglobulinemia 5",
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            "children": []
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            "id": "DOID:0080589",
            "label": "Klippel-Feil syndrome 1",
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            "children": []
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            "id": "DOID:0080591",
            "label": "Klippel-Feil syndrome 3",
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            "children": []
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            "id": "DOID:0080593",
            "label": "orofacial cleft 6",
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            "children": []
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            "id": "DOID:0080598",
            "label": "Kleefstra syndrome 2",
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            "children": []
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            "id": "DOID:0080606",
            "label": "anterior segment dysgenesis 1",
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            "children": []
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            "id": "DOID:0080608",
            "label": "anterior segment dysgenesis 3",
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            "children": []
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            "label": "anterior segment dysgenesis 4",
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            "children": []
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            "id": "DOID:0080625",
            "label": "severe congenital neutropenia 1",
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            "children": []
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            "label": "atrial standstill 1",
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            "children": []
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            "id": "DOID:0080664",
            "label": "diaphyseal medullary stenosis with malignant fibrous histiocytoma",
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            "children": []
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            "id": "DOID:0080666",
            "label": "warfarin sensitivity",
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            "children": []
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            "id": "DOID:0080669",
            "label": "posterior polymorphous corneal dystrophy 4",
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            "children": []
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            "id": "DOID:0080670",
            "label": "Meesmann corneal dystrophy 1",
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            "children": []
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            "id": "DOID:0080671",
            "label": "Meesmann corneal dystrophy 2",
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            "children": []
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            "id": "DOID:0080673",
            "label": "fibrochondrogenesis 2",
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            "children": []
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            "id": "DOID:0080675",
            "label": "Stickler syndrome 2",
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            "children": []
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            "id": "DOID:0080676",
            "label": "Stickler syndrome 1",
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            "children": []
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            "label": "otospondylomegaepiphyseal dysplasia, autosomal dominant",
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            "children": []
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            "id": "DOID:0080686",
            "label": "tubular aggregate myopathy 2",
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            "children": []
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            "id": "DOID:0080698",
            "label": "Teebi hypertelorism syndrome 1",
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            "children": []
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            "id": "DOID:0080719",
            "label": "congenital myopathy 6",
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            "children": []
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            "id": "DOID:0080720",
            "label": "autosomal dominant congenital deafness with onychodystrophy",
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            "children": []
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            "id": "DOID:0080723",
            "label": "Kenny-Caffey syndrome type 2",
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            "children": []
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            "id": "DOID:0080726",
            "label": "Ehlers-Danlos syndrome classic type 2",
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            "children": []
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            "id": "DOID:0080727",
            "label": "Ehlers-Danlos syndrome arthrochalasia type 1",
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            "children": []
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            "id": "DOID:0080728",
            "label": "Ehlers-Danlos syndrome arthrochalasia type 2",
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            "children": []
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            "id": "DOID:0080757",
            "label": "Fanconi renotubular syndrome 1",
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            "children": []
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            "id": "DOID:0080759",
            "label": "Fanconi renotubular syndrome 3",
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            "children": []
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            "id": "DOID:0080760",
            "label": "Fanconi renotubular syndrome 4",
            "link_status": true,
            "children": []
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            "id": "DOID:0080764",
            "label": "hereditary diffuse gastric cancer",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0080766",
            "label": "erythrokeratodermia variabilis et progressiva 6",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0080770",
            "label": "autosomal dominant beta thalassemia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0080773",
            "label": "delta beta-thalassemia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0080801",
            "label": "autosomal dominant craniometaphyseal dysplasia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0080807",
            "label": "autosomal dominant craniodiaphyseal dysplasia",
            "link_status": true,
            "children": []
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            "id": "DOID:0080837",
            "label": "growth hormone insensitivity syndrome with immune dysregulation 2",
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            "children": []
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            "id": "DOID:0080840",
            "label": "optic atrophy 12",
            "link_status": true,
            "children": []
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            "id": "DOID:0080845",
            "label": "omodysplasia 2",
            "link_status": true,
            "children": []
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            "id": "DOID:0080860",
            "label": "primary ovarian insufficiency 3",
            "link_status": true,
            "children": []
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            "id": "DOID:0080862",
            "label": "primary ovarian insufficiency 5",
            "link_status": true,
            "children": []
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            "id": "DOID:0080863",
            "label": "primary ovarian insufficiency 6",
            "link_status": true,
            "children": []
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            "id": "DOID:0080864",
            "label": "primary ovarian insufficiency 7",
            "link_status": true,
            "children": []
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            "id": "DOID:0080868",
            "label": "primary ovarian insufficiency 11",
            "link_status": true,
            "children": []
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            "id": "DOID:0080873",
            "label": "primary ovarian insufficiency 16",
            "link_status": true,
            "children": []
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            "id": "DOID:0080893",
            "label": "Bainbridge-Ropers syndrome",
            "link_status": true,
            "children": []
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            "id": "DOID:0080943",
            "label": "46,XX sex reversal 5",
            "link_status": true,
            "children": []
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            "id": "DOID:0080944",
            "label": "familial Behcet-like autoinflammatory syndrome",
            "link_status": true,
            "children": []
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            "label": "arrhythmogenic right ventricular dysplasia 14",
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            "id": "DOID:0080977",
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            "label": "Ehlers-Danlos syndrome periodontal type 1",
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            "id": "DOID:0080987",
            "label": "Ehlers-Danlos syndrome periodontal type 2",
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            "id": "DOID:0080990",
            "label": "King Denborough syndrome",
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            "id": "DOID:0081001",
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            "id": "DOID:0081002",
            "label": "Cowden syndrome 6",
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            "id": "DOID:0081003",
            "label": "Cowden syndrome 7",
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            "id": "DOID:0081030",
            "label": "central conducting lymphatic anomaly",
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            "id": "DOID:0081048",
            "label": "congenital limbs-face contractures-hypotonia-developmental delay syndrome",
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            "id": "DOID:0081061",
            "label": "nephrogenic diabetes insipidus type 2",
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            "id": "DOID:0081063",
            "label": "DICER1 syndrome",
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            "id": "DOID:0081075",
            "label": "Marsili syndrome",
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            "id": "DOID:0081079",
            "label": "ectodermal dysplasia and immunodeficiency 2",
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            "id": "DOID:0081101",
            "label": "nonautoimmune hyperthyroidism",
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            "id": "DOID:0081102",
            "label": "familial gestational hyperthyroidism",
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            "id": "DOID:0081108",
            "label": "keratosis palmoplantaris striata 1",
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            "id": "DOID:0081109",
            "label": "keratosis palmoplantaris striata 2",
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            "id": "DOID:0081110",
            "label": "keratosis palmoplantaris striata 3",
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            "id": "DOID:0081112",
            "label": "Baraitser-Winter syndrome 1",
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            "id": "DOID:0081113",
            "label": "Baraitser-Winter syndrome 2",
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            "label": "benign familial infantile seizures 2",
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            "label": "benign familial infantile seizures 3",
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            "label": "benign familial infantile seizures 5",
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            "id": "DOID:0081121",
            "label": "inclusion body myopathy and brain white matter abnormalities",
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            "id": "DOID:0081126",
            "label": "DeSanto-Shinawi syndrome",
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            "id": "DOID:0081133",
            "label": "3-methylglutaconic aciduria type 7a",
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            "id": "DOID:0081140",
            "label": "agammaglobulinemia 8A",
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            "id": "DOID:0081142",
            "label": "agammaglobulinemia 10",
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            "id": "DOID:0081145",
            "label": "common variable immunodeficiency 2",
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            "children": []
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            "id": "DOID:0081152",
            "label": "common variable immunodeficiency 10",
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            "children": []
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            "id": "DOID:0081154",
            "label": "common variable immunodeficiency 12",
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            "children": []
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            "id": "DOID:0081155",
            "label": "common variable immunodeficiency 13",
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            "children": []
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            "id": "DOID:0081156",
            "label": "common variable immunodeficiency 14",
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            "id": "DOID:0081157",
            "label": "dilated cardiomyopathy 1LL",
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            "children": []
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            "id": "DOID:0081158",
            "label": "dilated cardiomyopathy 1MM",
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            "id": "DOID:0081176",
            "label": "hypotonia, ataxia, and delayed development syndrome",
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            "id": "DOID:0081242",
            "label": "autoimmune interstitial lung, joint, and kidney disease",
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            "id": "DOID:0081268",
            "label": "pulmonary venoocclusive disease 1",
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            "id": "DOID:0081287",
            "label": "white sponge nevus 1",
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            "children": []
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            "id": "DOID:0081288",
            "label": "white sponge nevus 2",
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            "children": []
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            "id": "DOID:0081290",
            "label": "Antley-Bixler syndrome without disordered steroidogenesis",
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            "children": []
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            "id": "DOID:0081294",
            "label": "neuronal intranuclear inclusion disease",
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            "children": []
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            "id": "DOID:0081295",
            "label": "essential tremor 6",
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            "children": []
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            "id": "DOID:0081297",
            "label": "oculopharyngodistal myopathy 1",
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            "children": []
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            "id": "DOID:0081298",
            "label": "oculopharyngodistal myopathy 2",
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            "children": []
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            "id": "DOID:0081299",
            "label": "oculopharyngodistal myopathy 3",
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            "children": []
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            "id": "DOID:0081300",
            "label": "oculopharyngodistal myopathy 4",
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            "id": "DOID:0081301",
            "label": "intellectual developmental disorder with ocular anomalies and distinctive facial features",
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            "id": "DOID:0081321",
            "label": "contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A",
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            "children": []
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            "id": "DOID:0081336",
            "label": "Thomsen disease",
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            "children": []
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            "id": "DOID:0081340",
            "label": "congenital myopathy 2C",
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            "children": []
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            "id": "DOID:0081342",
            "label": "congenital myopathy 8",
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            "id": "DOID:0081347",
            "label": "congenital myopathy 15",
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            "id": "DOID:0081348",
            "label": "congenital myopathy 16",
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            "id": "DOID:0081350",
            "label": "congenital myopathy 18",
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            "id": "DOID:0081356",
            "label": "spinal muscular atrophy, Jokela type",
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            "children": []
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            "id": "DOID:0081357",
            "label": "isolated mitochondrial myopathy",
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            "children": []
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            "id": "DOID:0081358",
            "label": "epidermolytic hyperkeratosis 1",
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            "id": "DOID:0081363",
            "label": "distal myopathy with rimmed vacuoles",
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            "id": "DOID:0081365",
            "label": "Paget's disease of bone 2",
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            "children": []
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            "id": "DOID:0081366",
            "label": "Paget's disease of bone 3",
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            "children": []
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            "id": "DOID:0081369",
            "label": "Paget's disease of bone 6",
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            "children": []
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            "id": "DOID:0081371",
            "label": "lacrimoauriculodentodigital syndrome 2",
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            "children": []
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            "id": "DOID:0081372",
            "label": "lacrimoauriculodentodigital syndrome 3",
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            "children": []
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            "id": "DOID:0081375",
            "label": "nemaline myopathy 5C",
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            "children": []
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            "id": "DOID:0081378",
            "label": "amyotrophic lateral sclerosis type 24",
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            "children": []
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            "id": "DOID:0081379",
            "label": "amyotrophic lateral sclerosis type 25",
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            "children": []
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            "id": "DOID:0081380",
            "label": "amyotrophic lateral sclerosis type 26",
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            "children": []
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            "id": "DOID:0081381",
            "label": "juvenile amyotrophic lateral sclerosis type 27",
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            "children": []
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            "id": "DOID:0081382",
            "label": "amyotrophic lateral sclerosis type 28",
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            "children": []
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            "id": "DOID:0081395",
            "label": "Harel-Yoon syndrome",
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            "children": []
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            "id": "DOID:0081397",
            "label": "Vissers-Bodmer syndrome",
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            "children": []
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            "id": "DOID:0081398",
            "label": "holoprosencephaly 12",
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            "label": "familial focal epilepsy with variable foci",
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                    "label": "familial focal epilepsy with variable foci 2",
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                    "id": "DOID:0081423",
                    "label": "familial focal epilepsy with variable foci 3",
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                    "id": "DOID:0081424",
                    "label": "familial focal epilepsy with variable foci 4",
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            "id": "DOID:0081433",
            "label": "Peroxisome biogenesis disorder 4B",
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            "id": "DOID:0081441",
            "label": "Nicolaides-Baraitser syndrome",
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            "id": "DOID:0081442",
            "label": "blepharophimosis-impaired intellectual development syndrome",
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            "id": "DOID:0081449",
            "label": "cone-rod dystrophy 24",
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            "children": []
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            "id": "DOID:0090002",
            "label": "Tietz syndrome",
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            "children": []
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            "id": "DOID:0090006",
            "label": "renal coloboma syndrome",
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            "id": "DOID:0090018",
            "label": "TNF receptor\\u2013associated periodic syndrome",
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            "id": "DOID:0090021",
            "label": "split hand-foot malformation 1",
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            "id": "DOID:0090023",
            "label": "split hand-foot malformation 4",
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            "children": []
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            "id": "DOID:0090029",
            "label": "CINCA Syndrome",
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            "children": []
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            "id": "DOID:0090034",
            "label": "myoclonic dystonia 11",
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            "id": "DOID:0090036",
            "label": "myoclonic dystonia 26",
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            "children": []
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            "id": "DOID:0090039",
            "label": "torsion dystonia 6",
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            "children": []
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            "id": "DOID:0090041",
            "label": "torsion dystonia 4",
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            "children": []
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            "id": "DOID:0090043",
            "label": "dopa-responsive dystonia",
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            "id": "DOID:0090044",
            "label": "dystonia 9",
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            "children": []
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            "id": "DOID:0090045",
            "label": "glucose transporter type 1 deficiency syndrome 2",
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            "id": "DOID:0090049",
            "label": "paroxysmal nonkinesigenic dyskinesia 1",
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            "id": "DOID:0090052",
            "label": "dystonia 24",
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            "children": []
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            "id": "DOID:0090053",
            "label": "episodic kinesigenic dyskinesia 1",
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            "id": "DOID:0090055",
            "label": "dystonia 25",
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            "children": []
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            "id": "DOID:0090056",
            "label": "dystonia 12",
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            "children": []
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            "id": "DOID:0090062",
            "label": "familial cold autoinflammatory syndrome 1",
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            "children": []
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            "id": "DOID:0090063",
            "label": "familial cold autoinflammatory syndrome 2",
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            "children": []
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            "id": "DOID:0090064",
            "label": "familial cold autoinflammatory syndrome 3",
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            "children": []
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            "id": "DOID:0090065",
            "label": "familial cold autoinflammatory syndrome 4",
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            "children": []
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            "id": "DOID:0090069",
            "label": "giant axonal neuropathy 2",
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            "children": []
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            "id": "DOID:0090075",
            "label": "hypogonadotropic hypogonadism 15 with or without anosmia",
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            "children": []
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            "id": "DOID:0090076",
            "label": "hypogonadotropic hypogonadism 18 with or without anosmia",
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            "children": []
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            "id": "DOID:0090077",
            "label": "hypogonadotropic hypogonadism 4 with or without anosmia",
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            "children": []
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            "id": "DOID:0090079",
            "label": "hypogonadotropic hypogonadism 17 with or without anosmia",
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            "children": []
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            "id": "DOID:0090080",
            "label": "hypogonadotropic hypogonadism 16 with or without anosmia",
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            "children": []
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            "id": "DOID:0090082",
            "label": "hypogonadotropic hypogonadism 20 with or without anosmia",
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            "children": []
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            "id": "DOID:0090083",
            "label": "hypogonadotropic hypogonadism 2 with or without anosmia",
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            "children": []
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            "id": "DOID:0090084",
            "label": "hypogonadotropic hypogonadism 5 with or without anosmia",
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            "children": []
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            "id": "DOID:0090085",
            "label": "hypogonadotropic hypogonadism 9 with or without anosmia",
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            "children": []
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        {
            "id": "DOID:0090086",
            "label": "hypogonadotropic hypogonadism 6 with or without anosmia",
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            "children": []
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            "id": "DOID:0090087",
            "label": "hypogonadotropic hypogonadism 14 with or without anosmia",
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            "children": []
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            "id": "DOID:0090090",
            "label": "hypogonadotropic hypogonadism 19 with or without anosmia",
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            "children": []
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            "id": "DOID:0090092",
            "label": "hypogonadotropic hypogonadism 3 with or without anosmia",
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            "children": []
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            "id": "DOID:0090093",
            "label": "hypogonadotropic hypogonadism 21 with or without anosmia",
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            "children": []
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            "id": "DOID:0090100",
            "label": "ocular albinism with sensorineural deafness",
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            "children": []
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            "label": "autosomal dominant isolated macrothrombocytopenia 1",
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            "children": []
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            "id": "DOID:0090109",
            "label": "autosomal dominant hypocalcemia",
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                    "label": "autosomal dominant hypocalcemia 1",
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                    "children": []
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                    "id": "DOID:0090108",
                    "label": "autosomal dominant hypocalcemia 2",
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                    "children": []
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            "id": "DOID:0090111",
            "label": "PCWH syndrome",
            "link_status": true,
            "children": []
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            "id": "DOID:0090114",
            "label": "Sorsby's fundus dystrophy",
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            "children": []
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        {
            "id": "DOID:0090119",
            "label": "ankyloblepharon-ectodermal defects-cleft lip/palate syndrome",
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            "children": []
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            "id": "DOID:0090120",
            "label": "hereditary neutrophilia",
            "link_status": true,
            "children": []
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            "id": "DOID:0090125",
            "label": "brain small vessel disease 1",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0090132",
            "label": "complex cortical dysplasia with other brain malformations 7",
            "link_status": true,
            "children": []
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            "id": "DOID:0090133",
            "label": "complex cortical dysplasia with other brain malformations 2",
            "link_status": true,
            "children": []
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            "id": "DOID:0090134",
            "label": "complex cortical dysplasia with other brain malformations 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0090135",
            "label": "complex cortical dysplasia with other brain malformations 5",
            "link_status": true,
            "children": []
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            "id": "DOID:0090136",
            "label": "complex cortical dysplasia with other brain malformations 6",
            "link_status": true,
            "children": []
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            "id": "DOID:0090137",
            "label": "complex cortical dysplasia with other brain malformations 1",
            "link_status": true,
            "children": []
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            "id": "DOID:0090138",
            "label": "complex cortical dysplasia with other brain malformations 4",
            "link_status": true,
            "children": []
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            "id": "DOID:0090140",
            "label": "cortisone reductase deficiency 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0110032",
            "label": "Alport syndrome 3A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0110035",
            "label": "Alzheimer's disease 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0110040",
            "label": "Alzheimer's disease 4",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0110042",
            "label": "Alzheimer's disease 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110052",
            "label": "amelogenesis imperfecta type 1B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110053",
            "label": "amelogenesis imperfecta type 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110054",
            "label": "amelogenesis imperfecta type 1A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0110055",
            "label": "amelogenesis imperfecta type 3A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0110070",
            "label": "arrhythmogenic right ventricular dysplasia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110074",
            "label": "arrhythmogenic right ventricular dysplasia 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110076",
            "label": "arrhythmogenic right ventricular dysplasia 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110077",
            "label": "arrhythmogenic right ventricular dysplasia 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110081",
            "label": "arrhythmogenic right ventricular dysplasia 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110083",
            "label": "arrhythmogenic right ventricular dysplasia 12",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110084",
            "label": "arrhythmogenic right ventricular dysplasia 13",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110107",
            "label": "atrial heart septal defect 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110110",
            "label": "atrial heart septal defect 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110111",
            "label": "atrial heart septal defect 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110112",
            "label": "atrial heart septal defect 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110113",
            "label": "atrial heart septal defect 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110114",
            "label": "atrial heart septal defect 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110115",
            "label": "autoimmune lymphoproliferative syndrome type 2A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110117",
            "label": "autoimmune lymphoproliferative syndrome type 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110148",
            "label": "Charcot-Marie-Tooth disease type 1A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110149",
            "label": "Charcot-Marie-Tooth disease type 1F",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110150",
            "label": "Charcot-Marie-Tooth disease type 1D",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110151",
            "label": "Charcot-Marie-Tooth disease type 1C",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110152",
            "label": "Charcot-Marie-Tooth disease type 1B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110153",
            "label": "Charcot-Marie-Tooth disease type 1E",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110154",
            "label": "Charcot-Marie-Tooth disease type 2A1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110155",
            "label": "Charcot-Marie-Tooth disease type 2A2A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110157",
            "label": "Charcot-Marie-Tooth disease type 2J",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110158",
            "label": "Charcot-Marie-Tooth disease type 2I",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110159",
            "label": "Charcot-Marie-Tooth disease type 2B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110160",
            "label": "Charcot-Marie-Tooth disease axonal type 2T",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110162",
            "label": "Charcot-Marie-Tooth disease, axonal type 2W",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110163",
            "label": "Charcot-Marie-Tooth disease axonal type 2F",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110164",
            "label": "Charcot-Marie-Tooth disease type 2D",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110165",
            "label": "Charcot-Marie-Tooth disease type 2E",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110167",
            "label": "Charcot-Marie-Tooth disease axonal type 2K",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110168",
            "label": "Charcot-Marie-Tooth disease type 2Y",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110169",
            "label": "Charcot-Marie-Tooth disease axonal type 2P",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110170",
            "label": "Charcot-Marie-Tooth disease axonal type 2Q",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110173",
            "label": "Charcot-Marie-Tooth disease axonal type 2U",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110174",
            "label": "Charcot-Marie-Tooth disease axonal type 2L",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110175",
            "label": "Charcot-Marie-Tooth disease axonal type 2O",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110177",
            "label": "Charcot-Marie-Tooth disease axonal type 2N",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110178",
            "label": "Charcot-Marie-Tooth disease axonal type 2V",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110180",
            "label": "Charcot-Marie-Tooth disease axonal type 2CC",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110181",
            "label": "Charcot-Marie-Tooth disease axonal type 2Z",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110182",
            "label": "Charcot-Marie-Tooth disease axonal type 2C",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110195",
            "label": "congenital hypomyelinating neuropathy 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110197",
            "label": "Charcot-Marie-Tooth disease dominant intermediate B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110199",
            "label": "Charcot-Marie-Tooth disease dominant intermediate C",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110200",
            "label": "Charcot-Marie-Tooth disease dominant intermediate D",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110202",
            "label": "Charcot-Marie-Tooth disease dominant intermediate A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110205",
            "label": "Charcot-Marie-Tooth disease dominant intermediate E",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110206",
            "label": "Charcot-Marie-Tooth disease dominant intermediate F",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110216",
            "label": "Leber congenital amaurosis 11",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110218",
            "label": "Brugada syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110224",
            "label": "Brugada syndrome 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110226",
            "label": "Brugada syndrome 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110229",
            "label": "cataract 6 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110231",
            "label": "cataract 1 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110234",
            "label": "cataract 4 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110235",
            "label": "cataract 2 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110236",
            "label": "cataract 39 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110237",
            "label": "cataract 42",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110239",
            "label": "cataract 12 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110240",
            "label": "cataract 20 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110241",
            "label": "cataract 41",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110248",
            "label": "cataract 30",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110249",
            "label": "cataract 11 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110250",
            "label": "cataract 16 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110251",
            "label": "cataract 15 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110253",
            "label": "cataract 14 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110255",
            "label": "cataract 5 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110256",
            "label": "cataract 21 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110258",
            "label": "cataract 10 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110259",
            "label": "cataract 43",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110260",
            "label": "cataract 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110264",
            "label": "cataract 33",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110265",
            "label": "cataract 31 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110266",
            "label": "cataract 9 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110268",
            "label": "cataract 22 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110269",
            "label": "cataract 3 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110270",
            "label": "cataract 17 multiple types",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110273",
            "label": "autosomal dominant limb-girdle muscular dystrophy",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0110304",
                    "label": "autosomal dominant limb-girdle muscular dystrophy type 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110305",
                    "label": "autosomal dominant limb-girdle muscular dystrophy type 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110306",
                    "label": "autosomal dominant limb-girdle muscular dystrophy type 3",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0110330",
            "label": "Leber congenital amaurosis 13",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110334",
            "label": "osteogenesis imperfecta type 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110339",
            "label": "osteogenesis imperfecta type 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110340",
            "label": "osteogenesis imperfecta type 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110341",
            "label": "osteogenesis imperfecta type 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110344",
            "label": "osteogenesis imperfecta type 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110356",
            "label": "retinitis pigmentosa 18",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110357",
            "label": "retinitis pigmentosa 35",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110366",
            "label": "retinitis pigmentosa 33",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110372",
            "label": "retinitis pigmentosa 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110383",
            "label": "retinitis pigmentosa 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110386",
            "label": "retinitis pigmentosa 42",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110387",
            "label": "retinitis pigmentosa 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110388",
            "label": "retinitis pigmentosa 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110390",
            "label": "retinitis pigmentosa 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110392",
            "label": "retinitis pigmentosa 70",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110397",
            "label": "retinitis pigmentosa 27",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110399",
            "label": "retinitis pigmentosa 37",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110403",
            "label": "retinitis pigmentosa 13",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110404",
            "label": "retinitis pigmentosa 17",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110408",
            "label": "retinitis pigmentosa 11",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110411",
            "label": "retinitis pigmentosa 60",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110423",
            "label": "dilated cardiomyopathy 1C",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110424",
            "label": "dilated cardiomyopathy 1CC",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110425",
            "label": "dilated cardiomyopathy 1A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110426",
            "label": "dilated cardiomyopathy 1D",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110427",
            "label": "dilated cardiomyopathy 1V",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110428",
            "label": "dilated cardiomyopathy 1AA",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110432",
            "label": "dilated cardiomyopathy 1NN",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110433",
            "label": "dilated cardiomyopathy 1E",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110438",
            "label": "dilated cardiomyopathy 1JJ",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110443",
            "label": "dilated cardiomyopathy 1B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110445",
            "label": "dilated cardiomyopathy 1KK",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110447",
            "label": "dilated cardiomyopathy 1DD",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110448",
            "label": "dilated cardiomyopathy 1HH",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110450",
            "label": "dilated cardiomyopathy 1II",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110454",
            "label": "dilated cardiomyopathy 1S",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110455",
            "label": "dilated cardiomyopathy 1U",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110456",
            "label": "dilated cardiomyopathy 1R",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110457",
            "label": "dilated cardiomyopathy 1Y",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110640",
            "label": "congenital muscular dystrophy due to LMNA mutation",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110644",
            "label": "long QT syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110645",
            "label": "long QT syndrome 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110646",
            "label": "long QT syndrome 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110647",
            "label": "long QT syndrome 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110648",
            "label": "long QT syndrome 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110649",
            "label": "long QT syndrome 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110650",
            "label": "long QT syndrome 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110651",
            "label": "long QT syndrome 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110652",
            "label": "long QT syndrome 11",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110653",
            "label": "long QT syndrome 12",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110654",
            "label": "long QT syndrome 13",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110655",
            "label": "long QT syndrome 14",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110656",
            "label": "long QT syndrome 15",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110659",
            "label": "congenital myasthenic syndrome 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110662",
            "label": "congenital myasthenic syndrome 1B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110663",
            "label": "congenital myasthenic syndrome 1A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110666",
            "label": "congenital myasthenic syndrome 3A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110678",
            "label": "congenital myasthenic syndrome 4A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110681",
            "label": "congenital myasthenic syndrome 2A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110683",
            "label": "developmental and epileptic encephalopathy 117",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110698",
            "label": "hypotrichosis 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110699",
            "label": "hypotrichosis 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110700",
            "label": "hypotrichosis 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110701",
            "label": "hypotrichosis 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110702",
            "label": "hypotrichosis 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110708",
            "label": "hypotrichosis 11",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110709",
            "label": "hypotrichosis 12",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110710",
            "label": "hypotrichosis 13",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110715",
            "label": "congenital stationary night blindness autosomal dominant 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110720",
            "label": "neuronal ceroid lipofuscinosis 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110737",
            "label": "neurodegeneration with brain iron accumulation 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110741",
            "label": "type 1 diabetes mellitus 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110763",
            "label": "hereditary spastic paraplegia 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110765",
            "label": "hereditary spastic paraplegia 12",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110766",
            "label": "hereditary spastic paraplegia 13",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110770",
            "label": "hereditary spastic paraplegia 17",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110782",
            "label": "hereditary spastic paraplegia 31",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110791",
            "label": "hereditary spastic paraplegia 3A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110792",
            "label": "hereditary spastic paraplegia 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110794",
            "label": "hereditary spastic paraplegia 42",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110811",
            "label": "hereditary spastic paraplegia 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110817",
            "label": "hereditary spastic paraplegia 72A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110818",
            "label": "hereditary spastic paraplegia 73",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110823",
            "label": "hereditary spastic paraplegia 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110824",
            "label": "hereditary spastic paraplegia 9A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110855",
            "label": "posterior polymorphous corneal dystrophy 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110856",
            "label": "posterior polymorphous corneal dystrophy 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110862",
            "label": "congenital stationary night blindness autosomal dominant 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110863",
            "label": "congenital stationary night blindness autosomal dominant 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110872",
            "label": "holoprosencephaly 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110873",
            "label": "holoprosencephaly 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110875",
            "label": "holoprosencephaly 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110876",
            "label": "holoprosencephaly 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110877",
            "label": "holoprosencephaly 11",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110878",
            "label": "holoprosencephaly 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110880",
            "label": "holoprosencephaly 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110916",
            "label": "hereditary spherocytosis type 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110917",
            "label": "hereditary spherocytosis type 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110919",
            "label": "hereditary spherocytosis type 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110932",
            "label": "congenital myopathy 23",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110935",
            "label": "nemaline myopathy 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110937",
            "label": "autosomal dominant osteopetrosis 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110938",
            "label": "autosomal dominant osteopetrosis 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110964",
            "label": "brachydactyly type A1",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0110977",
                    "label": "brachydactyly type A1C",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110978",
                    "label": "brachydactyly type A1D",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:0110965",
            "label": "brachydactyly type A2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110970",
            "label": "brachydactyly type C",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110971",
            "label": "brachydactyly type D",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111035",
            "label": "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111036",
            "label": "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111049",
            "label": "platelet-type bleeding disorder 17",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111053",
            "label": "platelet-type bleeding disorder 15",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111055",
            "label": "platelet-type bleeding disorder 20",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111056",
            "label": "platelet-type bleeding disorder 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111074",
            "label": "progressive familial heart block type IA",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111076",
            "label": "progressive familial heart block type IB",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111078",
            "label": "tibial muscular dystrophy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111090",
            "label": "Fanconi anemia complementation group R",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111128",
            "label": "focal segmental glomerulosclerosis 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111129",
            "label": "focal segmental glomerulosclerosis 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111130",
            "label": "focal segmental glomerulosclerosis 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111132",
            "label": "focal segmental glomerulosclerosis 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111133",
            "label": "focal segmental glomerulosclerosis 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111150",
            "label": "autosomal dominant isolated ectopia lentis 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111158",
            "label": "SADDAN",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111161",
            "label": "Crouzon syndrome-acanthosis nigricans syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111168",
            "label": "sepiapterin reductase deficiency",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111170",
            "label": "autosomal dominant sensory ataxia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111189",
            "label": "distal myopathy 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111191",
            "label": "distal myopathy Tateyama type",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111195",
            "label": "erythrokeratodermia variabilis et progressiva 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111198",
            "label": "autosomal dominant distal hereditary motor neuronopathy",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0051042",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 15",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081399",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 10",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081400",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 11",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0081401",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 13",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111199",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 7",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111202",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 14",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111203",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 5",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111205",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 12",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111206",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111207",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 3",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111209",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111210",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111212",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 9",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111215",
                    "label": "autosomal dominant distal hereditary motor neuronopathy 8",
                    "link_status": true,
                    "children": []
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        {
            "id": "DOID:0111217",
            "label": "autosomal dominant centronuclear myopathy",
            "link_status": false,
            "children": [
                {
                    "id": "DOID:0111223",
                    "label": "centronuclear myopathy 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111224",
                    "label": "centronuclear myopathy 4",
                    "link_status": true,
                    "children": []
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        },
        {
            "id": "DOID:0111247",
            "label": "hypertension and brachydactyly syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111248",
            "label": "cerebrocostomandibular syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111249",
            "label": "uveal coloboma-cleft lip and palate-intellectual disability",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111256",
            "label": "hyperferritinemia-cataract syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111269",
            "label": "autosomal dominant hyaline body myopathy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111275",
            "label": "speech-language disorder-1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111331",
            "label": "intellectual disability-severe speech delay-mild dysmorphism syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111336",
            "label": "craniofacial-deafness-hand syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111338",
            "label": "isolated elevated serum creatine phosphokinase levels",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111339",
            "label": "Vohwinkel syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111340",
            "label": "dominant optic atrophy plus syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111341",
            "label": "primary failure of tooth eruption",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111342",
            "label": "dermatopathia pigmentosa reticularis",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111343",
            "label": "lateral meningocele syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111346",
            "label": "epidermolysis bullosa simplex 2F with mottled pigmentation",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111347",
            "label": "epidermolysis bullosa with congenital localized absence of skin and deformity of nails",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111348",
            "label": "multiple epiphyseal dysplasia with myopia and deafness",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111350",
            "label": "Laurin-Sandrow syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111352",
            "label": "D-2-hydroxyglutaric aciduria 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111357",
            "label": "adermatoglyphia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111358",
            "label": "Floating-Harbor syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111360",
            "label": "hypotrichosis-lymphedema-telangiectasia-renal defect syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111362",
            "label": "hawkinsinuria",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111363",
            "label": "Heinz body anemia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111364",
            "label": "Alzheimer's disease 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111365",
            "label": "benign familial hematuria",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111367",
            "label": "Beukes hip dysplasia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111369",
            "label": "hyperalphalipoproteinemia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111370",
            "label": "apolipoprotein C-III deficiency",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111373",
            "label": "familial progressive hyperpigmentation with or without hypopigmentation",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111374",
            "label": "selective pituitary thyroid hormone resistance",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111380",
            "label": "solitary median maxillary central incisor",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111381",
            "label": "IVIC syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111382",
            "label": "ischiocoxopodopatellar syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111383",
            "label": "autosomal dominant keratitis",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111384",
            "label": "inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111385",
            "label": "inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111386",
            "label": "inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111399",
            "label": "congenital dyserythropoietic anemia type IIIa",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111400",
            "label": "congenital dyserythropoietic anemia type IVa",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111403",
            "label": "mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111408",
            "label": "exudative vitreoretinopathy 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111410",
            "label": "exudative vitreoretinopathy 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111412",
            "label": "exudative vitreoretinopathy 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111428",
            "label": "essential tremor 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111431",
            "label": "essential tremor 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111432",
            "label": "essential tremor 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111433",
            "label": "optic atrophy 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111434",
            "label": "optic atrophy 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111438",
            "label": "optic atrophy 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111441",
            "label": "optic atrophy 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111447",
            "label": "progressive myoclonus epilepsy 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111454",
            "label": "SHORT syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111457",
            "label": "STING-associated vasculopathy with onset in infancy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111460",
            "label": "cardiofaciocutaneous syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111461",
            "label": "cardiofaciocutaneous syndrome 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111462",
            "label": "cardiofaciocutaneous syndrome 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111463",
            "label": "cardiofaciocutaneous syndrome 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111505",
            "label": "palmoplantar keratoderma-deafness syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111506",
            "label": "palmoplantar keratoderma-esophageal carcinoma syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111507",
            "label": "Lenz-Majewski hyperostotic dwarfism",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111509",
            "label": "lymphedema-distichiasis syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111511",
            "label": "melanoma and neural system tumor syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111512",
            "label": "metachondromatosis",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111513",
            "label": "metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome",
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            "children": []
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            "id": "DOID:0111514",
            "label": "metatropic dysplasia",
            "link_status": true,
            "children": []
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            "id": "DOID:0111517",
            "label": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2",
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            "children": []
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        {
            "id": "DOID:0111518",
            "label": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5",
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            "children": []
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        {
            "id": "DOID:0111519",
            "label": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6",
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            "children": []
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        {
            "id": "DOID:0111520",
            "label": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3",
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            "children": []
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        {
            "id": "DOID:0111521",
            "label": "autosomal dominant progressive external ophthalmoplegia 1",
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            "children": []
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        {
            "id": "DOID:0111525",
            "label": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4",
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            "children": []
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        {
            "id": "DOID:0111526",
            "label": "Mullerian aplasia and hyperandrogenism",
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            "children": []
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        {
            "id": "DOID:0111528",
            "label": "Naegeli-Franceschetti-Jadassohn syndrome",
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            "children": []
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        {
            "id": "DOID:0111531",
            "label": "bilateral optic nerve hypoplasia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111532",
            "label": "osteoglophonic dysplasia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111533",
            "label": "gnathodiaphyseal dysplasia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111534",
            "label": "multicentric carpotarsal osteolysis syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111535",
            "label": "progressive osseous heteroplasia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111536",
            "label": "Buschke-Ollendorff syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111537",
            "label": "paroxysmal extreme pain disorder",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111538",
            "label": "paramyotonia congenita of Von Eulenburg",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111539",
            "label": "parastremmatic dwarfism",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111541",
            "label": "pigmented paravenous chorioretinal atrophy",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111542",
            "label": "familial expansile osteolysis",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111543",
            "label": "juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111544",
            "label": "Guttmacher syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111545",
            "label": "familial male-limited precocious puberty",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111546",
            "label": "Currarino syndrome",
            "link_status": true,
            "children": []
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            "id": "DOID:0111547",
            "label": "retinal arterial tortuosity",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111548",
            "label": "ring dermoid of cornea",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111549",
            "label": "aplasia of lacrimal and salivary glands",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111550",
            "label": "scalp-ear-nipple syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111551",
            "label": "neurogenic scapuloperoneal syndrome Kaeser type",
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            "children": []
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            "id": "DOID:0111552",
            "label": "scapuloperoneal spinal muscular atrophy",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111553",
            "label": "spondyloepiphyseal dysplasia Maroteaux type",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111554",
            "label": "spondylometaphyseal dysplasia Kozlowski type",
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            "children": []
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        {
            "id": "DOID:0111556",
            "label": "steatocystoma multiplex",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111558",
            "label": "Charcot-Marie-Tooth disease type 2DD",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111560",
            "label": "Charcot-Marie-Tooth disease type 1G",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111561",
            "label": "stiff skin syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111562",
            "label": "overhydrated hereditary stomatocytosis",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111564",
            "label": "hypoplastic or aplastic tibia with polydactyly",
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            "children": []
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        {
            "id": "DOID:0111565",
            "label": "trichodontoosseous syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111567",
            "label": "retinal vasculopathy with cerebral leukodystrophy",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111568",
            "label": "congenital vertical talus",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111569",
            "label": "autosomal dominant vitreoretinochoroidopathy",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111570",
            "label": "snowflake vitreoretinal degeneration",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111571",
            "label": "Weyers acrofacial dysostosis",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111573",
            "label": "autosomal dominant woolly hair",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111576",
            "label": "dehydrated hereditary stomatocytosis 1",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111577",
            "label": "dehydrated hereditary stomatocytosis 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111581",
            "label": "C syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111584",
            "label": "dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome",
            "link_status": true,
            "children": []
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            "id": "DOID:0111595",
            "label": "congenital contractural arachnodactyly",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111597",
            "label": "distal arthrogryposis type 1A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111598",
            "label": "distal arthrogryposis type 1B",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111600",
            "label": "distal arthrogryposis type 2B1",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111601",
            "label": "distal arthrogryposis type 2B2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111602",
            "label": "distal arthrogryposis type 2B3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111603",
            "label": "distal arthrogryposis type 7",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111605",
            "label": "distal arthrogryposis type 2A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111607",
            "label": "distal arthrogryposis type 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111608",
            "label": "distal arthrogryposis type 5",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111647",
            "label": "Schopf-Schulz-Passarge syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111652",
            "label": "ectodermal dysplasia 12",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111653",
            "label": "ectodermal dysplasia 11A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111663",
            "label": "ectodermal dysplasia 10A",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111673",
            "label": "Saul-Wilson syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111675",
            "label": "neurooculocardiogenitourinary syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111682",
            "label": "cystic renal dysplasia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111683",
            "label": "neurofibromatosis-Noonan syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111686",
            "label": "hereditary mixed polyposis syndrome 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111688",
            "label": "Ayme-Gripp syndrome",
            "link_status": true,
            "children": []
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            "id": "DOID:0111690",
            "label": "familial adult myoclonic epilepsy 1",
            "link_status": true,
            "children": []
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            "id": "DOID:0111692",
            "label": "familial adult myoclonic epilepsy 2",
            "link_status": true,
            "children": []
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            "id": "DOID:0111693",
            "label": "familial adult myoclonic epilepsy 4",
            "link_status": true,
            "children": []
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            "id": "DOID:0111694",
            "label": "familial adult myoclonic epilepsy 7",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111695",
            "label": "familial adult myoclonic epilepsy 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111696",
            "label": "familial adult myoclonic epilepsy 6",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111697",
            "label": "cleft palate, cardiac defects, and intellectual disability",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111700",
            "label": "ankyrin-B-related cardiac arrhythmia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111706",
            "label": "oblique facial clefting 1",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111707",
            "label": "Bothnian type palmoplantar keratoderma",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111709",
            "label": "focal nonepidermolytic palmoplantar keratoderma 1",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111710",
            "label": "focal or diffuse nonepidermolytic palmoplantar keratoderma",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111711",
            "label": "focal nonepidermolytic palmoplantar keratoderma 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111726",
            "label": "geleophysic dysplasia 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111727",
            "label": "geleophysic dysplasia 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111729",
            "label": "familial episodic pain syndrome 1",
            "link_status": true,
            "children": []
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            "id": "DOID:0111730",
            "label": "familial episodic pain syndrome 2",
            "link_status": true,
            "children": []
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            "id": "DOID:0111731",
            "label": "familial episodic pain syndrome 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111733",
            "label": "pancreatic hypoplasia-diabetes-congenital heart disease syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111763",
            "label": "46,XX sex reversal 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111764",
            "label": "46,XX sex reversal 4",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111769",
            "label": "46,XY sex reversal 6",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111770",
            "label": "46,XY sex reversal 9",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111772",
            "label": "46,XY sex reversal 3",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111775",
            "label": "46,XY sex reversal 10",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111787",
            "label": "frontometaphyseal dysplasia 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0111801",
            "label": "syndromic microphthalmia 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111805",
            "label": "syndromic microphthalmia 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111806",
            "label": "syndromic microphthalmia 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111816",
            "label": "syndactyly type 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111817",
            "label": "syndactyly type 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111818",
            "label": "syndactyly type 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111819",
            "label": "syndactyly type 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111837",
            "label": "congenital nongoitrous hypothyroidism 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111856",
            "label": "primary ciliary dyskinesia 43",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111878",
            "label": "Diamond-Blackfan anemia 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111879",
            "label": "Diamond-Blackfan anemia 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111880",
            "label": "Diamond-Blackfan anemia 17",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111881",
            "label": "Diamond-Blackfan anemia 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111882",
            "label": "Diamond-Blackfan anemia 12",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111883",
            "label": "Diamond-Blackfan anemia 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111884",
            "label": "Diamond-Blackfan anemia 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111886",
            "label": "Diamond-Blackfan anemia 19",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111887",
            "label": "Diamond-blackfan anemia 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111888",
            "label": "Diamond-Blackfan anemia 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111889",
            "label": "Diamond-Blackfan anemia 13",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111890",
            "label": "Diamond-Blackfan anemia 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111891",
            "label": "Diamond-Blackfan anemia 20",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111892",
            "label": "Diamond-Blackfan anemia 11",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111893",
            "label": "Diamond-Blackfan anemia 16",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111894",
            "label": "Diamond-Blackfan anemia 15 with mandibulofacial dysostosis",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111895",
            "label": "Diamond-Blackfan anemia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111896",
            "label": "Diamond-Blackfan anemia 18",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111900",
            "label": "autosomal dominant thrombophilia due to protein S deficiency",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111901",
            "label": "heparin cofactor II deficiency",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111902",
            "label": "thrombophilia due to activated protein C resistance",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111903",
            "label": "thrombophilia due to HRG deficiency",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111907",
            "label": "thrombophilia due to thrombin defect",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111921",
            "label": "spermatogenic failure 36",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111925",
            "label": "spermatogenic failure 32",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111931",
            "label": "syndactyly-telecanthus-anogenital and renal malformations syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111936",
            "label": "immunodeficiency 14",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111945",
            "label": "immunodeficiency 31A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111946",
            "label": "immunodeficiency 31C",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111947",
            "label": "immunodeficiency 21",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111949",
            "label": "immunodeficiency 36",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111954",
            "label": "immunodeficiency 60",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111956",
            "label": "immunodeficiency 27B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111958",
            "label": "immunodeficiency 11B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111960",
            "label": "immunodeficiency 15A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111969",
            "label": "immunodeficiency 39",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111979",
            "label": "immunodeficiency 49",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111986",
            "label": "immunodeficiency 32A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111987",
            "label": "immunodeficiency 13",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112005",
            "label": "immunodeficiency 70",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112013",
            "label": "autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112014",
            "label": "congenital megabladder",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112061",
            "label": "immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia",
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            "children": []
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        {
            "id": "DOID:0112064",
            "label": "immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis",
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            "children": []
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        {
            "id": "DOID:0112102",
            "label": "Sotos syndrome 2",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112103",
            "label": "Sotos syndrome 1",
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            "children": []
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            "id": "DOID:0112130",
            "label": "autosomal dominant severe congenital neutropenia",
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                {
                    "id": "DOID:0112131",
                    "label": "severe congenital neutropenia 2",
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                    "children": []
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                {
                    "id": "DOID:0112135",
                    "label": "severe congenital neutropenia 8",
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                    "children": []
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        {
            "id": "DOID:0112140",
            "label": "retinitis pigmentosa 83",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112144",
            "label": "retinitis pigmentosa 87",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112146",
            "label": "retinitis pigmentosa 89",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112149",
            "label": "terminal osseous dysplasia",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112154",
            "label": "inflammatory bowel disease 30",
            "link_status": true,
            "children": []
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            "id": "DOID:0112155",
            "label": "inflammatory bowel disease 29",
            "link_status": true,
            "children": []
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            "id": "DOID:0112161",
            "label": "Noonan syndrome 13",
            "link_status": true,
            "children": []
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            "id": "DOID:0112169",
            "label": "Noonan syndrome 11",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112170",
            "label": "Noonan syndrome 12",
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            "children": []
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        {
            "id": "DOID:0112195",
            "label": "spondyloperipheral dysplasia",
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            "children": []
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            "id": "DOID:0112199",
            "label": "spondyloepimetaphyseal dysplasia with joint laxity type 2",
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            "children": []
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            "id": "DOID:0112203",
            "label": "developmental and epileptic encephalopathy 67",
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            "children": []
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            "id": "DOID:0112205",
            "label": "developmental and epileptic encephalopathy 69",
            "link_status": true,
            "children": []
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            "id": "DOID:0112206",
            "label": "developmental and epileptic encephalopathy 70",
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            "children": []
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        {
            "id": "DOID:0112208",
            "label": "developmental and epileptic encephalopathy 72",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112209",
            "label": "developmental and epileptic encephalopathy 73",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112210",
            "label": "developmental and epileptic encephalopathy 74",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112214",
            "label": "developmental and epileptic encephalopathy 78",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112215",
            "label": "developmental and epileptic encephalopathy 79",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112221",
            "label": "developmental and epileptic encephalopathy 87",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112226",
            "label": "Bosch-Boonstra-Schaaf optic atrophy syndrome",
            "link_status": true,
            "children": []
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        {
            "id": "DOID:0112228",
            "label": "lissencephaly 9 with complex brainstem malformation",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112229",
            "label": "lissencephaly 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112232",
            "label": "lissencephaly 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112237",
            "label": "lissencephaly 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112240",
            "label": "Leber congenital amaurosis with early-onset deafness",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112242",
            "label": "congenital symmetric circumferential skin creases 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112243",
            "label": "congenital symmetric circumferential skin creases 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112247",
            "label": "congenital heart defects, dysmorphic facial features, and intellectual developmental disorder",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112262",
            "label": "leucine-sensitive hypoglycemia of infancy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112263",
            "label": "hypoinsulinemic hypoglycemia with hemihypertrophy",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112275",
            "label": "developmental and epileptic encephalopathy 93",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112276",
            "label": "neurodevelopmental disorder with involuntary movements",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112281",
            "label": "spondyloepiphyseal dysplasia Stanescu type",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112282",
            "label": "spondyloepiphyseal dysplasia Kimberley type",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112297",
            "label": "spondylometaphyseal dysplasia corner fracture type",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112309",
            "label": "central precocious puberty 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112310",
            "label": "central precocious puberty 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112314",
            "label": "autosomal dominant brain small vessel disease 2A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112339",
            "label": "Tatton-Brown-Rahman syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112341",
            "label": "hereditary spastic paraplegia 80",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112359",
            "label": "congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112383",
            "label": "KINSSHIP syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:10016",
            "label": "multiple endocrine neoplasia type 2B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:10017",
            "label": "multiple endocrine neoplasia type 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:10041",
            "label": "dysplastic nevus syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:10383",
            "label": "amyotrophic neuralgia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:1068",
            "label": "juvenile glaucoma",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:10871",
            "label": "age related macular degeneration",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0050817",
                    "label": "Stargardt disease",
                    "link_status": true,
                    "children": [
                        {
                            "id": "DOID:0061238",
                            "label": "Stargardt disease 3",
                            "link_status": true,
                            "children": []
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                        {
                            "id": "DOID:0061239",
                            "label": "Stargardt disease 4",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0061240",
                            "label": "Stargardt disease 5",
                            "link_status": true,
                            "children": []
                        },
                        {
                            "id": "DOID:0061241",
                            "label": "Stargardt disease 1",
                            "link_status": true,
                            "children": []
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                    ]
                },
                {
                    "id": "DOID:0110014",
                    "label": "age related macular degeneration 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110015",
                    "label": "age related macular degeneration 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110017",
                    "label": "age related macular degeneration 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110018",
                    "label": "age related macular degeneration 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110019",
                    "label": "age related macular degeneration 7",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110020",
                    "label": "age related macular degeneration 8",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110021",
                    "label": "age related macular degeneration 9",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110023",
                    "label": "age related macular degeneration 11",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110024",
                    "label": "age related macular degeneration 12",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110025",
                    "label": "age related macular degeneration 13",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110026",
                    "label": "age related macular degeneration 14",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110027",
                    "label": "age related macular degeneration 15",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110028",
                    "label": "age related macular degeneration 5",
                    "link_status": true,
                    "children": []
                }
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        },
        {
            "id": "DOID:11198",
            "label": "DiGeorge syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:11661",
            "label": "blue color blindness",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:12185",
            "label": "otosclerosis",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0060928",
                    "label": "otosclerosis 11",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:12318",
            "label": "granular corneal dystrophy",
            "link_status": false,
            "children": [
                {
                    "id": "DOID:0060444",
                    "label": "granular corneal dystrophy 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080530",
                    "label": "granular corneal dystrophy 1",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:12388",
            "label": "neurohypophyseal diabetes insipidus",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:1270",
            "label": "hereditary hemorrhagic telangiectasia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:13374",
            "label": "fibrodysplasia ossificans progressiva",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:13515",
            "label": "tuberous sclerosis",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0080324",
                    "label": "tuberous sclerosis 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080325",
                    "label": "tuberous sclerosis 2",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:13994",
            "label": "cleidocranial dysplasia",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:14291",
            "label": "Noonan syndrome with multiple lentigines",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0080548",
                    "label": "Noonan syndrome with multiple lentigines 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080549",
                    "label": "Noonan syndrome with multiple lentigines 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080550",
                    "label": "Noonan syndrome with multiple lentigines 3",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:1441",
            "label": "autosomal dominant cerebellar ataxia",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0050882",
                    "label": "spinocerebellar ataxia 5",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050954",
                    "label": "spinocerebellar ataxia 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050955",
                    "label": "spinocerebellar ataxia 2",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050956",
                    "label": "spinocerebellar ataxia 6",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050957",
                    "label": "spinocerebellar ataxia 4",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050958",
                    "label": "spinocerebellar ataxia 7",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050959",
                    "label": "spinocerebellar ataxia 8",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050960",
                    "label": "spinocerebellar ataxia 10",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050961",
                    "label": "spinocerebellar ataxia 11",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050962",
                    "label": "spinocerebellar ataxia 12",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050963",
                    "label": "spinocerebellar ataxia 13",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050964",
                    "label": "spinocerebellar ataxia 14",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050965",
                    "label": "spinocerebellar ataxia 15",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050967",
                    "label": "spinocerebellar ataxia 17",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050968",
                    "label": "autosomal dominant cerebellar ataxia, deafness and narcolepsy",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050970",
                    "label": "spinocerebellar ataxia 19/22",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050971",
                    "label": "spinocerebellar ataxia 20",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050972",
                    "label": "spinocerebellar ataxia 21",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050973",
                    "label": "spinocerebellar ataxia 23",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050974",
                    "label": "spinocerebellar ataxia 25",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050975",
                    "label": "spinocerebellar ataxia 26",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050976",
                    "label": "spinocerebellar ataxia 27A",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050977",
                    "label": "spinocerebellar ataxia 28",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050978",
                    "label": "spinocerebellar ataxia 29",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050980",
                    "label": "spinocerebellar ataxia 31",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050981",
                    "label": "spinocerebellar ataxia 34",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050982",
                    "label": "spinocerebellar ataxia 35",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050983",
                    "label": "spinocerebellar ataxia 36",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050984",
                    "label": "spinocerebellar ataxia 37",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050985",
                    "label": "spinocerebellar ataxia 38",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050986",
                    "label": "spinocerebellar ataxia 40",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050987",
                    "label": "hypomyelinating leukoencephalopathy",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0050998",
                    "label": "nonprogressive cerebellar ataxia with mental retardation",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0060162",
                    "label": "dentatorubral-pallidoluysian atrophy",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0061137",
                    "label": "spinocerebellar ataxia 27B",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080286",
                    "label": "spinocerebellar ataxia 44",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080287",
                    "label": "spinocerebellar ataxia 45",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0080288",
                    "label": "spinocerebellar ataxia 46",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111742",
                    "label": "cerebellar ataxia type 42",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111743",
                    "label": "cerebellar ataxia type 47",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111744",
                    "label": "cerebellar ataxia type 41",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111745",
                    "label": "cerebellar ataxia type 43",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111746",
                    "label": "cerebellar ataxia type 48",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:1440",
                    "label": "Machado-Joseph disease",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:14686",
            "label": "Axenfeld-Rieger syndrome",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0110120",
                    "label": "Axenfeld-Rieger syndrome type 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0110122",
                    "label": "Axenfeld-Rieger syndrome type 3",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:14693",
            "label": "Clouston syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:14702",
            "label": "branchiootorenal syndrome",
            "link_status": true,
            "children": [
                {
                    "id": "DOID:0111423",
                    "label": "branchiootorenal syndrome 1",
                    "link_status": true,
                    "children": []
                },
                {
                    "id": "DOID:0111424",
                    "label": "branchiootorenal syndrome 2",
                    "link_status": true,
                    "children": []
                }
            ]
        },
        {
            "id": "DOID:14705",
            "label": "Pfeiffer syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:14720",
            "label": "Ehlers-Danlos syndrome classic type 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:14731",
            "label": "Weaver syndrome",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:14735",
            "label": "hereditary angioedema",
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