{
    "disease_id": "DOID:0050569",
    "recommended_name": {
        "id": "DOID:0050569",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050569",
        "name": "Seckel syndrome",
        "description": "A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability."
    },
    "synonyms": [
        {
            "id": "DOID:0050569",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050569",
            "name": "Harper's syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050569",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050569",
            "name": "Virchow-Seckel dwarfism",
            "description": ""
        },
        {
            "id": "DOID:0050569",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050569",
            "name": "bird-headed dwarfism",
            "description": ""
        },
        {
            "id": "DOID:0050569",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050569",
            "name": "microcephalic primordial dwarfism",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome 1",
            "description": "Any Seckel syndrome in which the cause of the disease is a mutation in the ATR gene."
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "ATR Seckel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "SCKL1",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome caused by mutation in ATR",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome type 1",
            "description": ""
        },
        {
            "id": "MIM:210600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/210600",
            "name": "Seckel syndrome 1",
            "description": "Seckel syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0070005",
            "label": "Seckel syndrome 9",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070006",
            "label": "Seckel syndrome 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070007",
            "label": "Seckel syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070008",
            "label": "Seckel syndrome 10",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070009",
            "label": "Seckel syndrome 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070010",
            "label": "Seckel syndrome 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070011",
            "label": "Seckel syndrome 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070012",
            "label": "Seckel syndrome 5",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070013",
            "label": "Seckel syndrome 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070013",
        "DOID:0070012",
        "DOID:0070005",
        "DOID:0070009",
        "DOID:0050569",
        "DOID:0070010",
        "DOID:0070008",
        "DOID:0070006",
        "DOID:0070011",
        "DOID:0070007"
    ],
    "unlinked_id_list": []
}