{
    "disease_id": "DOID:0111387",
    "recommended_name": {
        "id": "DOID:0111387",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111387",
        "name": "familial isolated hypoparathyroidism",
        "description": "A hypoparathyroidism that has_material_basis_in mutation in PTH on chromosome 6p24.2 or in GCM2 on chromosome 11p15.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111387",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111387",
            "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": "hypoparathyroidism, familial isolated",
            "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": "hypoparathyroidism, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "hypoparathyroidism, familial isolated; FIH",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "hypoparathyroidism, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0007796",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007796",
            "name": "FIH",
            "description": ""
        },
        {
            "id": "MIM:146200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/146200",
            "name": "Hypoparathyroidism, familial isolated, 1",
            "description": "Hypoparathyroidism, familial isolated, 1"
        }
    ]
}