ARHGAP42

Rho GTPase activating protein 42
OMIM: 615936, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red ARHGAP42 in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 4.202
Latest signed off version: v4.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Interstitial lung disease
  • systemic hypertension
  • immunological abnormalities