OSM

oncostatin M
OMIM: 165095, Gene2Phenotype

1 panel

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


Level 2: Immunology
Version 9.37
Latest signed off version: v9.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • bone marrow disorder, MONDO:0003225