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Summary Literature (0)
DOID:0080207 - CAKUT2

Disease Ontology Definition:A CAKUT that has_material_basis_in heterozygous mutation in the TBX18 gene on chromosome 6q14.

Synonyms: Congenital anomalies of the kidney and urinary tract 2

Xenbase Genes : tbx18

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0027676 - congenital anomalies of kidney and urinary tract 2


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): CAKUT (is_a)