{
    "disease_id": "DOID:0111836", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111836", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111836", 
            "name": "CHNG7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111836", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111836", 
            "name": "central hypothyroidism due to TRH receptor deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111836", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111836", 
            "name": "TRH resistance syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111836", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111836", 
            "name": "resistance to thyrotropin-releasing hormone syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111836", 
        "description": "A congenital hypothyroidism characterized by normal-to-low T4 and normal-to-high thyrotropin levels, with reduced or absent pituitary responsiveness to thyrotropin-releasing hormone that has_material_basis_in homozygous or compound heterozygous mutation in TRHR on chromosome 8q23.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111836", 
        "name": "congenital nongoitrous hypothyroidism 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111836#disease-associations", 
            "id": "0111836", 
            "database": "Alliance of Genome Resources"
        }
    ]
}