{
    "disease_id": "DOID:0070128", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013757", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013757", 
            "name": "congenital nongoitrous hypothryoidism 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013757", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013757", 
            "name": "hypothyroidism, congenital, nongoitrous, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013757", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013757", 
            "name": "hypothyroidism, congenital, nongoitrous caused by mutation in THRA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013757", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013757", 
            "name": "hypothyroidism, congenital, nongoitrous, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013757", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013757", 
            "name": "CHNG6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013757", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013757", 
            "name": "hypothyroidism, congenital, nongoitrous, 6; CHNG6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013757", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013757", 
            "name": "THRA hypothyroidism, congenital, nongoitrous"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070128", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070128", 
            "name": "CHNG6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070128", 
        "description": "A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070128", 
        "name": "congenital nongoitrous hypothyroidism 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070128#disease-associations", 
            "id": "0070128", 
            "database": "Alliance of Genome Resources"
        }
    ]
}