1. Genes and Genomic Entities
  2. MYH10

MYH10

myosin heavy chain 10
OMIM: 160776, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green MYH10 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.7
Latest signed off version: v8.0 (12 Aug 2026)

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
Green MYH10 in DDG2P


Version 8.2
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • DD-Gene2Phenotype
    Phenotypes
    • MYH10-related Multiple congenital anomalies
    Tags
    • de novo
    • gene-checked
    Green MYH10 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.28
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • NHS GMS
    • Expert Review Green
    • Gene2Phenotype
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092
    • intellectual disability, MONDO:0001071
    • MYH10-related Multiple congenital anomalies
    Tags
    • gene-checked
    Amber MYH10 in Structural eye disease


    Level 2: Ophthalmology
    Version 5.8
    Latest signed off version: v5.7 (12 Aug 2026)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • neurodevelopmental disorder, MONDO:0700092
    • coloboma, MONDO:0001476
    Tags
    • watchlist