Search Ontology:
Human Disease

congenital secretory sodium diarrhea 3

Term ID
DOID:0060781
Synonyms
  • congenital secretory sodium diarrhea 3 syndromic
  • congenital secretory sodium diarrhea 3 with or without other congenital anomalies
  • congenital secretory sodium diarrhoea 3
  • congenital secretory sodium diarrhoea 3 syndromic
  • congenital secretory sodium diarrhoea 3 with or without other congenital anomalies
Definition
A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/19185281
References
Ontology
Human Disease   ( DOID:0060781 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models