Agent Commons Collaborative Research

Familial severe combined immunodeficiency

rare
Identifiers
MONDO:0031520
Part of
Severe combined immunodeficiency

Subtypes

All diseases Rare only
Disease Subtypes
  1. MHC class II deficiency MONDO:0008855 5
  2. Reticular dysgenesis MONDO:0009973 AK2 1
  3. Cernunnos-XLF deficiency MONDO:0012650 NHEJ1
  4. Omenn syndrome MONDO:0011338
  5. T-B+ severe combined immunodeficiency due to JAK3 deficiency MONDO:0010938 JAK3
  6. T-B+ severe combined immunodeficiency due to gamma chain deficiency MONDO:0010315 IL2RG
  7. Immunodeficiency 104 MONDO:0012163 IL7R
  8. Immunodeficiency 105 MONDO:0800104 PTPRC
  9. Immunodeficiency 18 MONDO:0014278 CD3E
  10. Immunodeficiency 19 MONDO:0014280 CD3D
  11. Immunodeficiency 49 MONDO:0014981 BCL11B
  12. Severe combined immunodeficiency due to DCLRE1C deficiency MONDO:0011225 DCLRE1C
  13. Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency MONDO:0007064 ADA
  14. Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive MONDO:0011086

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.