TNFRSF13C

TNF receptor superfamily member 13C
OMIM: 606269, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber TNFRSF13C in Predominantly Antibody Deficiency


Level 2: Immunological disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Victorian Clinical Genetics Services
  • Melbourne Genomics Health Alliance Immunology Flagship
  • Expert Review Amber
  • Expert Review Amber
Phenotypes
  • Immunodeficiency, common variable, 4, MIM# 613494

Amber TNFRSF13C in Common Variable Immunodeficiency


Level 2: Immunological disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Victorian Clinical Genetics Services
  • Melbourne Genomics Health Alliance Immunology Flagship
  • Expert Review Amber
Phenotypes
  • Immunodeficiency, common variable, 4, MIM# 613494