Search Ontology:
Human Disease

congenital nongoitrous hypothyroidism 1

Term ID
DOID:0070126
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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