CAKUT1

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Summary

Literature (0)

DOID:0080206 - CAKUT1

Disease Ontology Definition:A CAKUT that has_material_basis_in heterozygous mutation in the DSTYK gene on chromosome 1q32.

Synonyms: Congenital anomalies of the kidney and urinary tract 1

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: dstyk

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012561 - congenital anomalies of kidney and urinary tract 1

MONDO:0012561 - congenital anomalies of kidney and urinary tract 1

MIM:

MIM:610805 - CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 1; CAKUT1

MIM:610805 - CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 1; CAKUT1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): CAKUT (is_a)