genetic disease of the immune system
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More general terms
More specific terms
- agammaglobulinemia type 2
- antiphospholipid syndrome (APS); Hughes syndrome
- autoimmune lymphoproliferative syndrome (ALPS, Canale-Smith syndrome)
- autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED); autoimmune polyglandular syndrome type 1; Whitaker's syndrome
- Chediak-Higashi syndrome
- combined immune deficiency; severe combined immunodeficiency disease (SCID CID)
- complement C2 deficiency
- eosinophil peroxidase deficiency
- familial candidiasis
- familial histiocytic reticulosis; familial hemophagocytic reticulosis; familial hemophagocytic lymphohistiocytosis; familial erythrophagocytic lymphohistiocytosis
- ficolin-3 deficiency
- Griscelli syndrome
- hereditary periodic fever syndrome; periodic fevers; recurrent fever syndrome; familial autoinflammatory disease
- hyper IgE recurrent infection syndrome autosomal recessive
- hypoglobulinemia & absent B-cells
- IRAK4 deficiency
- LFA-1 immunodeficiency disease
- Mendelian susceptibility to mycobacterial disease (MSMD); familial disseminated atypical mycobacterial infection
- recurrent invasive pneumococcal disease
- STAT1 deficiency