{
    "disease_id": "DOID:0061150",
    "recommended_name": {
        "id": "DOID:0061150",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061150",
        "name": "familial isolated hypoparathyroidism 1",
        "description": "A familial isolated hypoparathyroidism that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the parathyroid hormone PTH gene on chromosome 11p15."
    },
    "synonyms": [
        {
            "id": "DOID:0061150",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061150",
            "name": "FIH1",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "hypoparathyroidism, familial isolated 1",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "FIH",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "hypoparathyroidism, familial isolated",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "FIH1",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "hypoparathyroidism, familial isolated 1",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "hypoparathyroidism familial isolated",
            "description": ""
        },
        {
            "id": "MIM:146200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/146200",
            "name": "Hypoparathyroidism, familial isolated, 1",
            "description": "Hypoparathyroidism, familial isolated, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061150"
    ],
    "unlinked_id_list": []
}