{
    "disease_id": "DOID:0090108",
    "recommended_name": {
        "id": "DOID:0090108",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0090108",
        "name": "autosomal dominant hypocalcemia 2",
        "description": "An autosomal dominant hypocalcemia that has_material_basis_in heterozygous mutation in the G protein subunit alpha 11 gene (GNA11) on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "DOID:0090108",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0090108",
            "name": "HYPOC2",
            "description": ""
        },
        {
            "id": "MONDO:0014146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014146",
            "name": "autosomal dominant hypocalcemia 2",
            "description": "An autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13."
        },
        {
            "id": "MONDO:0014146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014146",
            "name": "HYPOC2",
            "description": ""
        },
        {
            "id": "MONDO:0014146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014146",
            "name": "autosomal dominant hypocalcemia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0014146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014146",
            "name": "hypocalcemia, autosomal dominant type 2",
            "description": ""
        },
        {
            "id": "MONDO:0014146",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014146",
            "name": "hypocalcemia, autosomal dominant 2",
            "description": ""
        },
        {
            "id": "MIM:615361",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615361",
            "name": "Hypocalcemia, autosomal dominant 2",
            "description": "Hypocalcemia, autosomal dominant 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0090108"
    ],
    "unlinked_id_list": []
}