ZFIN Human Disease: congenital secretory sodium diarrhea 3

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:	ICD10CM:P78.3 OMIM:270420 ORDO:103908
Ontology:	Human Disease ( DOID:0060781 )

Relationships

is a type of:	autosomal recessive disease physical disorder secretory diarrhea autosomal recessive disease physical disorder secretory diarrhea Show first 5 Terms

OTHER congenital secretory sodium diarrhea 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SPINT2	spint2	Diarrhea 3, secretory sodium, congenital, syndromic	270420

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None