MYH10

myosin heavy chain 10
OMIM: 160776
PanelMode of inheritanceDetails
1 panel
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
MYH10-related Multiple congenital anomalies, Bilateral ventriculomegaly, aqueductal stenosis