{
    "disease_id": "DOID:0111388", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010618", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010618", 
            "name": "familial isolated hypoparathyroidism due to agenesis of parathyroid gland"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010618", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010618", 
            "name": "parathyroid glands, agenesis of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010618", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010618", 
            "name": "hypoparathyroidism, X-linked; HYPX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010618", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010618", 
            "name": "HYPX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010618", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010618", 
            "name": "hypoparathyroidism, X-linked"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111388", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111388", 
            "name": "HYPX"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111388", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111388", 
            "name": "agenesis of parathyroid glands"
        }, 
        {
            "url": "https://www.omim.org/entry/307700", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:307700", 
            "name": "Hypoparathyroidism, X-linked"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111388", 
        "description": "A hypoparathyroidism that has_material_basis_in mutation in a region on chromosome Xq27.1 that appears to alter expression of SOX3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111388", 
        "name": "X-linked hypoparathyroidism"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/307700", 
            "id": "307700", 
            "database": "MIM"
        }
    ]
}