PanelApp (stage)
  1. Genes and Genomic Entities
  2. MYH8

MYH8

myosin heavy chain 8
OMIM: 160741, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green MYH8 in Arthrogryposis


Level 2: Neurology and neurodevelopmental disorders
Version 0.411

Component of the following Super Panels:

  • Neuromuscular Superpanel

    		•  review Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green MYH8 in Mendeliome


    Version 1.1891

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Trismus-pseudocamptodactyly syndrome MIM# 158300
    • Carney complex variant MIM# 608837

    Green MYH8 in Fetal anomalies


    Version 1.255

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Trismus-pseudocamptodactyly syndrome (MIM#158300)