OBO ID: DOID:0070126 |
Term Name: | congenital nongoitrous hypothyroidism 1 | Search Ontology: | |
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Definition: | A congenital hypothyroidism that has_material_basis_in mutation in the TSHR gene on chromosome 14q31. https://www.ncbi.nlm.nih.gov/pubmed/8954020 | ||
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Ontology: | Human Disease ( DOID:0070126 ) |
OTHER congenital nongoitrous hypothyroidism 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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