ZFIN Human Disease: congenital secretory chloride diarrhea 1

OBO ID: DOID:0060296

Term Name:	congenital secretory chloride diarrhea 1		Search Ontology:
Synonyms:	congenital chloride diarrhea finnish type congenital chloride diarrhoea finnish type congenital chloridorrhea congenital secretory chloride diarrhoea 1
Definition:	A secretory diarrhea that has_material_basis_in mutation in the SLC26A3 gene. https://omim.org/entry/214700
References:	MESH:C536210 OMIM:214700 ORDO:53689 SNOMEDCT_US_2023_03_01:24412005 UMLS_CUI:C0267662
Ontology:	Human Disease ( DOID:0060296 )

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 chloride diarrhea 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SLC26A3	slc26a3.2 slc26a3.1	Diarrhea 1, secretory chloride, congenital	214700

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None