OBO ID: DOID:0070128
Term Name: congenital nongoitrous hypothyroidism 6 Search Ontology:
Synonyms:
  • CHNG6
Definition: A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1. https://www.ncbi.nlm.nih.gov/pubmed/22168587
References:
Ontology: Human Disease   (DOID:0070128)
OTHER congenital nongoitrous hypothyroidism 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
THRA Hypothyroidism, congenital, nongoitrous, 6 614450
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None