PanelApp (staging)
  1. Genes and Genomic Entities
  2. MYO9B

MYO9B

myosin IXB
OMIM: 602129, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber MYO9B in Mendeliome


Version 1.2302

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Charcot-Marie-Tooth disease type 2 (MONDO:0018993), MYO9B-related

Amber MYO9B in Hereditary Neuropathy_CMT - isolated


Level 2: Neurology and neurodevelopmental disorders
Version 1.51

Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Charcot-Marie-Tooth disease type 2 (MONDO:0018993), MYO9B-related