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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:

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

In Mondo Disease Ontology:
MONDO:0012561 - congenital anomalies of kidney and urinary tract 1, susceptibility to

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : dstyk

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): CAKUT (is_a)