{
    "disease_id": "DOID:0090109",
    "recommended_name": {
        "id": "DOID:0090109",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0090109",
        "name": "autosomal dominant hypocalcemia",
        "description": "A metal metabolism disorder characterized by autosomal dominant inheritance of variable degrees of hypocalcemia with normal to low levels of parathyroid hormone."
    },
    "synonyms": [
        {
            "id": "DOID:0090109",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090109",
            "name": "HYPOC",
            "description": ""
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "autosomal dominant hypocalcemia 1",
            "description": "Any autosomal dominant hypocalcemia in which the cause of the disease is a mutation in the CASR gene."
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "hypocalcemia, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "CASR autosomal dominant hypocalcemia",
            "description": ""
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "HYPOC1",
            "description": ""
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "autosomal dominant hypocalcemia caused by mutation in CASR",
            "description": ""
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "autosomal dominant hypocalcemia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "hypocalcemia, autosomal dominant type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "hypocalcemia, autosomal dominant, with Bartter syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011013",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011013",
            "name": "hypocalcemia, autosomal dominant 1",
            "description": ""
        },
        {
            "id": "MIM:601198",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601198",
            "name": "Hypocalcemia, autosomal dominant 1",
            "description": "Hypocalcemia, autosomal dominant 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0090107",
            "label": "autosomal dominant hypocalcemia 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0090108",
            "label": "autosomal dominant hypocalcemia 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0090109",
        "DOID:0090108",
        "DOID:0090107"
    ],
    "unlinked_id_list": []
}