Genomics England
GMS Panels
Panels
Genes and Entities

MYO7A

myosin VIIA
OMIM: 276903
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
USHER SYNDROME TYPE 1B 276900, DEAFNESS AUTOSOMAL RECESSIVE TYPE 2 600060
Green
in Monogenic hearing loss
R-numbers: R67
Signed-off version 3.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
hearing loss, Usher syndrome, type 1B, 276900, Nonsyndromic Hearing Loss, Dominant, #600060:Deafness, autosomal recessive 2, Nonsyndromic Hearing Loss, Recessive, #601317:Deafness, autosomal dominant 11
Green
in Retinal disorders
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Eye Disorders