{
    "disease_id": "DOID:0060699",
    "recommended_name": {
        "id": "DOID:0060699",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060699",
        "name": "familial hypocalciuric hypercalcemia",
        "description": "A hypercalcemia characterized by autosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion."
    },
    "synonyms": [
        {
            "id": "DOID:0060699",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060699",
            "name": "FBH",
            "description": ""
        },
        {
            "id": "DOID:0060699",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060699",
            "name": "FBHH",
            "description": ""
        },
        {
            "id": "DOID:0060699",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060699",
            "name": "FHH",
            "description": ""
        },
        {
            "id": "DOID:0060699",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060699",
            "name": "familial benign hypercalcemia",
            "description": ""
        },
        {
            "id": "DOID:0060699",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060699",
            "name": "familial benign hypocalciuric hypercalcemia",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "familial hypocalciuric hypercalcemia 1",
            "description": "Any familial hypocalciuric hypercalcemia in which the cause of the disease is a mutation in the CASR gene."
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "CASR familial hypocalciuric hypercalcemia",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "FHH type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "HHC1",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "familial benign hypercalcemia 1",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "familial hypocalciuric hypercalcemia caused by mutation in CASR",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "familial hypocalciuric hypercalcemia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "hpocalciuric hypercalcemia, type I",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "FBH1",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "familial benign hypercalcemia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "hypercalcemia, familial benign type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "hypocalciuric hypercalcemia, familial, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007791",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007791",
            "name": "hypocalciuric hypercalcemia, familial, type I",
            "description": ""
        },
        {
            "id": "MIM:145980",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/145980",
            "name": "Hypocalciuric hypercalcemia, familial 1",
            "description": "Hypocalciuric hypercalcemia, familial 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0060700",
            "label": "familial hypocalciuric hypercalcemia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060701",
            "label": "familial hypocalciuric hypercalcemia 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060702",
            "label": "familial hypocalciuric hypercalcemia 3",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0060702",
        "DOID:0060699",
        "DOID:0060700",
        "DOID:0060701"
    ],
    "unlinked_id_list": []
}