Search Ontology:
Human Disease

congenital nongoitrous hypothyroidism 6

Term ID
DOID:0070128
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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