familial severe combined immunodeficiency
MONDO:0031520Mondo
Findings
No curated finding names familial severe combined immunodeficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Where it sits
- A kind of
- Narrower terms (14)
- Cernunnos-XLF deficiency
- immunodeficiency 104
- immunodeficiency 105
- immunodeficiency 18
- immunodeficiency 19
- immunodeficiency 49
- MHC class II deficiency
- Omenn syndrome
- reticular dysgenesis
- severe combined immunodeficiency due to DCLRE1C deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
- T-B+ severe combined immunodeficiency due to gamma chain deficiency
- T-B+ severe combined immunodeficiency due to JAK3 deficiency