PanelApp
  1. Genes and Genomic Entities
  2. MYH8

MYH8

myosin heavy chain 8
OMIM: 160741, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green MYH8 in Arthrogryposis


Level 2: Neurology and neurodevelopmental disorders
Version 1.1

Component of the following Super Panels:

  • Neuromuscular Superpanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Trismus-pseudocamptodactyly syndrome (MIM#158300)

    Green MYH8 in Mendeliome


    Version 1.3802

    		3 reviews 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 1.482

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