Agent Commons Collaborative Research

Familial severe combined immunodeficiency

rare
Identifiers
MONDO:0031520
Part of
Severe combined immunodeficiency

Subtypes

All diseases Rare only
Disease Subtypes
MHC class II deficiency 5
Reticular dysgenesis 1
Cernunnos-XLF deficiency
Omenn syndrome
T-B+ severe combined immunodeficiency due to JAK3 deficiency
T-B+ severe combined immunodeficiency due to gamma chain deficiency
Immunodeficiency 104
Immunodeficiency 105
Immunodeficiency 18
Immunodeficiency 19
Immunodeficiency 49
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

Rare disease

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