Genomics England
GMS Panels
Panels
Genes and Entities

MYH10

myosin heavy chain 10
OMIM: 160776
PanelMode of inheritanceDetails
2 panels
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
MYH10-related Multiple congenital anomalies, Bilateral ventriculomegaly, aqueductal stenosis
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.13
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Neurodevelopmental disorder, MONDO:0700092, intellectual disability, MONDO:0001071, MYH10-related Multiple congenital anomalies