Immunodeficiency 19
MONDO:0014280Any severe combined immunodeficiency in which the cause of the disease is a mutation in the CD3D gene.
Also known as: CD3D severe combined immunodeficiency (disease), CD3delta deficiency, immunodeficiency 19, immunodeficiency type 19, severe combined immunodeficiency (disease) caused by mutation in CD3D, CD3-Delta deficiency, IMD19, SCID, T cell-negative, B cell-positive, NK cell-positive
2 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsBroader 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)