Search Ontology:
Human Disease

congenital nongoitrous hypothyroidism 5

Term ID
DOID:0070125
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 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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