TBX18

PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CAKUT, Congenital anomalies of kidney and urinary tract 2, 143400
R-numbers: R257
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Congenital anomalies of kidney and urinary tract 2 143400