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Echinobase
Summary Literature (0)
DOID:0060781 - congenital secretory sodium diarrhea 3

Disease Ontology Definition:A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13.

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,

Echinobase Genes :


OMIM:
MIM:270420 - diarrhea 3, secretory sodium, congenital; diar3

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)