OBO ID: DOID:0070126
Term Name: congenital nongoitrous hypothyroidism 1 Search Ontology:
Synonyms:
  • CHNG1
  • TSH resistance
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
References:
Ontology: Human Disease   (DOID:0070126)
OTHER congenital nongoitrous hypothyroidism 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TSHR Hypothyroidism, congenital, nongoitrous, 1 275200
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None