TNFSF13

TNF superfamily member 13
OMIM: 604472, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red TNFSF13 in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 4.201
Latest signed off version: v4.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • APRIL deficiency
  • Common variable immunodeficiency