TNFSF12

TNF superfamily member 12
OMIM: 602695, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red TNFSF12 in Predominantly Antibody Deficiency


Level 2: Immunological disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Melbourne Genomics Health Alliance Immunology Flagship
  • Expert Review Red
Phenotypes
  • Inborn error of immunity, MONDO:0003778, TNFSF12-related

Red TNFSF12 in Common Variable Immunodeficiency


Level 2: Immunological disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Melbourne Genomics Health Alliance Immunology Flagship
  • Expert Review Red
Phenotypes
  • Inborn error of immunity, MONDO:0003778, TNFSF12-related