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Familial severe combined immunodeficiency

MONDO:0031520

24 clinical trials for this condition and its sub-types.

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Sub-types

T-B+ severe combined immunodeficiency due to gamma chain deficiency (10) Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency (6) Omenn syndrome (4) Severe combined immunodeficiency due to DCLRE1C deficiency (3) Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive (2) T-B+ severe combined immunodeficiency due to JAK3 deficiency (2) MHC class II deficiency (1) Reticular dysgenesis (1) Cernunnos-XLF deficiency (0) Immunodeficiency 104 (0) Immunodeficiency 105 (0) Immunodeficiency 18 (0) Immunodeficiency 19 (0) Immunodeficiency 49 (0) Immunoerythromyeloid hypoplasia (0) MHC class II deficiency 1 (0) MHC class II deficiency 2 (0) MHC class II deficiency 3 (0) MHC class II deficiency 4 (0) MHC class II deficiency 5 (0)

Broader categories

Disease (717) Hereditary disease (188) Immune system disorder (150) Immunodeficiency disease (55) Severe combined immunodeficiency (23) Human disease (15) Combined immunodeficiency (3) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 6 Not yet recruiting 2 Not yet finished but already full! 11 Completed 4 Terminated 1
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