Concept information
Preferred term
Primary immune deficiency disorder
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- 2'-5'-oligoadenylate synthetase 1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia
- Autoimmune lymphoproliferative syndrome
- Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
- CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome (disorder)
- Disorder of complement
- Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome (disorder)
- Immunoglobulin deficiency (disorder)
- Infantile inflammatory bowel disease with neurological involvement (disorder)
- Interleukin 21 related infantile inflammatory bowel disease (disorder)
- MSMD - mendelian susceptibility to mycobacterial disease
- NFAT5 (nuclear factor of activated T cells 5) haploinsufficiency
- Predisposition to invasive fungal disease due to CARD9 deficiency
- WILD syndrome
- X-linked immunoneurologic disorder (disorder)
- X-linked lymphoproliferative syndrome
Pathological process
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/58606001
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