Familial severe combined immunodeficiency
MONDO:003152037 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-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)
T-B+ severe combined immunodeficiency due to JAK3 deficiency
(2)
MHC class II deficiency
(1)
Reticular dysgenesis
(1)
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
(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
(618)
Hereditary disease
(172)
Immune system disorder
(140)
Immunodeficiency disease
(48)
Severe combined immunodeficiency
(21)
Human disease
(14)
Combined immunodeficiency
(3)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by etiologic mechanism
(0)