{
    "disease_id": "DOID:0070125", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009154", 
            "name": "hypothyroidism, congenital, nongoitrous, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009154", 
            "name": "CHNG5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009154", 
            "name": "hypothyroidism, congenital, nongoitrous, 5; CHNG5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009154", 
            "name": "NKX2-5 hypothyroidism, congenital, nongoitrous"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009154", 
            "name": "hypothyroidism, congenital, nongoitrous, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009154", 
            "name": "congenital nongoitrous hypothryoidism 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009154", 
            "name": "hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070125", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070125", 
            "name": "CHNG5"
        }, 
        {
            "url": "https://www.omim.org/entry/225250", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:225250", 
            "name": "Hypothyroidism, congenital, non-goitrous, 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070125", 
        "description": "A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the NKX2-5 gene on chromosome 5q35.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070125", 
        "name": "congenital nongoitrous hypothyroidism 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/225250", 
            "id": "225250", 
            "database": "MIM"
        }
    ]
}