FGL2

fibrinogen like 2
OMIM: 605351, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FGL2 in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 9.9
Latest signed off version: v9.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • autoinflammatory syndrome, MONDO:0019751