{
    "disease_id": "DOID:0111387", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007796", 
            "name": "hypoparathyroidism, familial isolated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007796", 
            "name": "hypoparathyroidism familial isolated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007796", 
            "name": "hypoparathyroidism, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007796", 
            "name": "hypoparathyroidism, familial isolated; FIH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007796", 
            "name": "hypoparathyroidism, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007796", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007796", 
            "name": "FIH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111387", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111387", 
            "name": "FIH"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111387", 
        "description": "A hypoparathyroidism that has_material_basis_in mutation in PTH on chromosome 6p24.2 or in GCM2 on chromosome 11p15.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111387", 
        "name": "familial isolated hypoparathyroidism"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111387#disease-associations", 
            "id": "0111387", 
            "database": "Alliance of Genome Resources"
        }
    ]
}