| OBO ID: DOID:0070127 |
| Term Name: | congenital nongoitrous hypothyroidism 3 | Search Ontology: | |
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| Definition: | A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has_material_basis_in variation in the chromosome region 15q25.3-q26.1. (2) | ||
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| Ontology: | Human Disease ( DOID:0070127 ) |
Show first 5 Terms
OTHER congenital nongoitrous hypothyroidism 3 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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