MYO6

PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.57
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Nonsyndromic Hearing Loss, Dominant, Deafness, autosomal dominant 22, 606346, Nonsyndromic Hearing Loss, Recessive, #606346:Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, #607821:Deafness, autosomal recessive 37