ZFIN Human Disease: congenital secretory sodium diarrhea 8

OBO ID: DOID:0060777

Term Name:	congenital secretory sodium diarrhea 8		Search Ontology:
Synonyms:	DIAR8
Definition:	A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SLC9A3 gene on chromosome 5p15. https://www.ncbi.nlm.nih.gov/pubmed/26358773
References:	ICD10CM:P78.3 OMIM:616868 ORDO:103908
Ontology:	Human Disease ( DOID:0060777 )

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 8 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SLC9A3	slc9a3.1 slc9a3.2	Diarrhea 8, secretory sodium, congenital	616868

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None