MYH11

myosin heavy chain 11
OMIM: 160745
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIH)
R-numbers: R438
Signed-off version 1.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Megacystis-microcolon-intestinal hypoperistalsis syndrome 2, OMIM:619351, Visceral myopathy 2, OMIM:619350
R-numbers: R125
Signed-off version 3.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Aortic aneurysm, familial thoracic 4, 132900, Aortic aneurysm, familial thoracic 4 (132900)