GIMAP5

GTPase, IMAP family member 5
OMIM: 608086, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber GIMAP5 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 Amber
  • Literature
Phenotypes
  • Portal hypertension, noncirrhotic, 2, OMIM:619463
  • lymphopenia
  • autoimmunity
  • immunodeficiency
  • liver disease
Tags
  • treatable
  • watchlist