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Autoimmune lymphoproliferative syndrome type "1," autosomal recessive
- ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but ... syndrome National Organization for Rare Disorders ( ...
- ... IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1 AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3 IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10 IMMUNODEFICIENCY, ...
- Resources about some of the forms of primary immune deficiency diseases (PIDDs) which NIAID is currently studying. ... Immune System and Disorders/Specifics ...
- Immune System and Disorders/Specifics ... Immune System and Disorders ... NIAID researches congenital neutropenia syndromes, a group of rare disorders present from ...
- Immune System and Disorders/Specifics ... Immune System and Disorders ... DOCK8 deficiency is a rare immune disorder named after the mutated gene which NIAID scientists ...
- Immune System and Disorders/Specifics ... Immune System and Disorders ... National Institute of Allergy and Infectious Diseases ... From the National Institutes of Health
- Primary Immune Deficiency Disease Genetics and Inheritance
(National Institute of Allergy and Infectious Diseases)
Immune System and Disorders/Genetics ... Immune System and Disorders ... National Institute of Allergy and Infectious Diseases ... From the National Institutes of Health