Primary Immune Deficiency Treatment Consortium (PIDTC)

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History Study of SCID Disorders	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA repair disease, Infant, Newborn, Diseases, Nutritional and Metabolic Diseases, Omenn syndrome, Primary Immunodeficiency Diseases, X-Linked Combined Immunodeficiency Diseases, X-linked disease, hereditary disease, immune system disorder, inborn error of immunity, metabolic disease, reticular dysgenesis, severe combined immunodeficiency, severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency	Enrolling by invitation	Not stated	2020-11-10		NCT01186913

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