MYH10

myosin heavy chain 10
OMIM: 160776, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red MYH10 in Autism Version 0.36	review	Not set	Sources Expert Review Red SFARI
Green MYH10 in Fetal anomalies Version 3.164 Latest signed off version: v3.0 (22 Mar 2023)	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Literature Expert Review Green Phenotypes MYH10-related Multiple congenital anomalies Bilateral ventriculomegaly aqueductal stenosis Tags gene-checked
Red MYH10 in DDG2P Version 3.88 Latest signed off version: v3.1 (22 Mar 2023) Component of the following Super Panels: Paediatric disorders	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources DD-Gene2Phenotype Expert Review Red Phenotypes MYH10-related Multiple congenital anomalies
Amber MYH10 in Intellectual disability - microarray and sequencing Level 3: Neurodevelopmental disorders Level 2: Neurology and neurodevelopmental disorders Version 5.544 Latest signed off version: v5.0 (22 Mar 2023) Component of the following Super Panels: Childhood onset leukodystrophy Hypotonic infant Paediatric disorders	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Gene2Phenotype Phenotypes Neurodevelopmental disorder, MONDO:0700092 intellectual disability, MONDO:0001071 MYH10-related Multiple congenital anomalies Tags Q4_23_promote_green
Green MYH10 in Severe Paediatric Disorders Version 1.184	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Next Generation Children Project Expert Review Green Expert list Phenotypes aqueductal stenosis MYH10-related Multiple congenital anomalies Bilateral ventriculomegaly