OBO ID: DOID:0070125
Term Name: congenital nongoitrous hypothyroidism 5 Search Ontology:
Synonyms:
  • CHNG5
Definition: A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the NKX2-5 gene on chromosome 5q35. https://www.ncbi.nlm.nih.gov/pubmed/16418214
References:
Ontology: Human Disease   ( DOID:0070125 )
OTHER congenital nongoitrous hypothyroidism 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NKX2-5 Hypothyroidism, congenital nongoitrous, 5 225250
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None