ARHGAP19

Rho GTPase activating protein 19
OMIM: 611587, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green ARHGAP19 in Mendeliome


Version 1.3490

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Motor Peripheral Neuropathy
  • MONDO:0002316
  • ARHGAP19 related

Green ARHGAP19 in Hereditary Neuropathy_CMT - isolated


Level 2: Neurology and neurodevelopmental disorders
Version 1.68

Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Motor Peripheral Neuropathy
    • MONDO:0002316
    • ARHGAP19 related