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Combined immunodeficiency
- JAK3-deficient severe combined immunodeficiency (SCID) is an inherited disorder of the immune system. Individuals with JAK3-deficient SCID lack the necessary ...
- X-linked severe combined immunodeficiency (SCID) is an inherited disorder of the immune system that occurs almost exclusively in males. Children with X- ...
- ZAP70-related severe combined immunodeficiency (SCID) is an inherited disorder that damages the immune system. ZAP70-related SCID is one of several forms of ...
- ... the immune system categorized as a form of combined immunodeficiency (CID). People with BLS II lack virtually all ... 2-negative SCID, HLA class II-negative Severe combined immunodeficiency due to absent class II human leukocyte antigens ...
- ... been identified in people with X-linked severe combined immunodeficiency (SCID). This condition is an inherited disorder of ... 2 receptor, gamma interleukin 2 receptor, gamma (severe combined immunodeficiency) SCIDX SCIDX1 X-SCID XSCID γc Tests of ...
- ... and nail dystrophy is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized ... cell immunodeficiency, congenital alopecia, and nail dystrophy Severe combined immunodeficiency due to FOXN1 deficiency National Organization for Rare ...
- ... hyper-IgE syndrome CID due to DOCK8 deficiency Combined immunodeficiency due to DOCK8 deficiency DOCK8 deficiency Hyper IgE ... Non-skeletal hyper-IgE syndrome Genetic Testing Registry: Combined immunodeficiency due to DOCK8 deficiency Combined immunodeficiency due to ...
- ... not show signs and symptoms of the condition. Combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia Roifman-Melamed syndrome ... Roifman CM, Melamed I. A novel syndrome of combined immunodeficiency, autoimmunity and spondylometaphyseal dysplasia. Clin Genet. 2003 Jun; ...
- ... condition. AGM1 deficiency CID due to PGM3 deficiency Combined immunodeficiency due to PGM3 deficiency Deficiency of N-acetylglucosamine- ...
- ... of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population. Ann ...