{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "CHNG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "resistance to thyrotropin"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "congenital nongoitrous hypothryoidism 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "hypothyroidism, congenital, due to thyroid dysgenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "thyrotropin resistance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "hypothyroidism, athyreotic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "congenital hypothyroidism due to thyroid dysgenesis or hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "thyroid, ectopic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "athyreotic hypothyroidism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "hypothyroidism, congenital, nongoitrous, 2; CHNG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024264", 
            "name": "thyroid dysgenesis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070124", 
            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "CHNG2"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070124", 
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        }, 
        {
            "url": "https://www.omim.org/entry/218700", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:218700", 
            "name": "Hypothyroidism, congenital, non-goitrous, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070124", 
        "description": "A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the PAX8 gene on chromosome 2q13.", 
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        "name": "congenital nongoitrous hypothyroidism 2"
    }, 
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            "id": "218700", 
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        }
    ]
}