MYOCD

PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 2.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Megabladder, congenital, OMIM:618719, Megabladder, congenital, MONDO:0032879
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Megabladder, congenital, OMIM:618719, Megabladder, congenital, MONDO:0032879