OBO ID: DOID:0060781
Term Name: congenital secretory sodium diarrhea 3 Search Ontology:
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)
OTHER congenital secretory sodium diarrhea 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPINT2 Diarrhea 3, secretory sodium, congenital, syndromic 270420
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None