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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
Echinobase Genes

MIM:610805 - congenital anomalies of kidney and urinary tract, susceptibility to; cakut |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
CAKUT (is_a)