Immunodeficiency 105
MONDO:0800104Any immunodeficiency disease which the cause of the disease is a mutation in the PTPRC gene.
Also known as: IMD105, SCID, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive, severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive
2 clinical trials for this condition and its sub-types.
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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)