{
    "disease_id": "DOID:0111835", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111835", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111835", 
            "name": "CHNG9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111835", 
        "description": "A congenital hypothyroidism characterized by a small thyroid gland with low free T4 levels and inappropriately normal levels of thyroid-stimulating hormone that has_material_basis_in hemizygous mutation in IRS4 on chromosome Xq22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111835", 
        "name": "congenital nongoitrous hypothyroidism 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111835#disease-associations", 
            "id": "0111835", 
            "database": "Alliance of Genome Resources"
        }
    ]
}