Disease #05341 (CAKUT2 (kidney and urinary tract, anomalies, congenital, type 2 (CAKUT-2)), OMIM:143400)

Official abbreviation	CAKUT2
Name	kidney and urinary tract, anomalies, congenital, type 2 (CAKUT-2)
OMIM ID	143400
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TBX18
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-11-10 19:47:53 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD