MYH8

myosin heavy chain 8
OMIM: 160741
PanelMode of inheritanceDetails
4 panels
R-numbers: R83
Signed-off version 3.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Trismus-pseudocamptodactyly syndrome (ARTHROGRYPOSIS, DISTAL, TYPE 7, DA7) 158300
Component of the following Super Panels:
  • - Hypotonic infant
  • - Neuromuscular disorders
R-numbers: R81
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Trismus-pseudocamptodactyly syndrome, 158300
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
DISTAL ARTHROGRYPOSIS TYPE 158300, CARNEY COMPLEX VARIANT 608837
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
DISTAL ARTHROGRYPOSIS TYPE, CARNEY COMPLEX VARIANT