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| Term | congenital nongoitrous hypothyroidism 6 | ID (Ontology) | DOID:0070128 (Human Disease) |
| Definition | A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1. | ||
| Also Known As | "CHNG6" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ physical disorder | |__congenital hypothyroidism___| hypothyroidism | |__congenital hypothyroidism___| congenital nongoitrous hypothyroidism 6 |
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| Is a |
congenital hypothyroidism autosomal dominant disease |
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External Crossreferences & Linkouts
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ICD10CM:E03.1 MIM:614450 |
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