FMNL2

formin like 2
OMIM: 616285, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FMNL2 in Primary immunodeficiency or monogenic inflammatory bowel disease


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

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • inflammatory bowel disease, MONDO:0005265