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Summary Literature (3)
DOID:0060296 - congenital secretory chloride diarrhea 1

Disease Ontology Definition:A secretory diarrhea that has_material_basis_in mutation in the SLC26A3 gene.

Synonyms: congenital chloride diarrhea finnish type, congenital chloride diarrhoea finnish type, congenital chloridorrhea, congenital secretory chloride diarrhoea 1,

Xenbase Genes : slc26a3.2, slc26a3.1, slc26a3.3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008964 - congenital secretory chloride diarrhea 1


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), physical disorder (is_a), secretory diarrhea (is_a)