PanelApp
  1. Genes and Genomic Entities
  2. MYH7B

MYH7B

myosin heavy chain 7B
OMIM: 609928, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber MYH7B in Hypertrophic cardiomyopathy


Level 2: Cardiovascular disorders
Version 2.0

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    Phenotypes
    • Hypertrophic cardiomyopathy, MONDO:0005045, MYH7B-related

    Amber MYH7B in Mendeliome


    Version 2.61

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Hypertrophic cardiomyopathy, MONDO:0005045, MYH7B-related
    • Hearing loss disorder, MONDO:0005365, MYH7B-related