Immunodeficiency: Difference between revisions
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{{Family tree| | | | | | | | | | | | | | | | | A01 | | | | | | | | |A01=Immunodeficiency}} | {{Family tree| | | | | | | | | | | | | | | | | A01 | | | | | | | | |A01=Immunodeficiency}} | ||
{{Family tree| |,|-|-|-|v|-|-|-|v|-|-|-|v|-|-|-|+|-|-|-|v|-|-|-|v|-|-|-|v|-|-|-|.| }} | {{Family tree| |,|-|-|-|v|-|-|-|v|-|-|-|v|-|-|-|+|-|-|-|v|-|-|-|v|-|-|-|v|-|-|-|.| }} | ||
{{Family tree| B01 | | B02 | | B03 | | B04 | | B05 | | B06 | | B07 | | B08 | | B09 | |B01=Immunodeficiency affecting cellular and humoral Immunity|B02=Combined immunodeficiency|B03=Predominantly antibody deficiency|B04=Diseases of immune dysregulation|B05=Congenital defects of phagocytes|B06=Defects in intrinsic and innate immunity|B07=Auto- | {{Family tree| B01 | | B02 | | B03 | | B04 | | B05 | | B06 | | B07 | | B08 | | B09 | |B01=[[Immunodeficiency affecting cellular and humoral Immunity]]|B02=[[Combined immunodeficiency]]|B03=[[Predominantly antibody deficiency]]|B04=[[Diseases of immune dysregulation]]|B05=[[Congenital defects of phagocytes]]|B06=[[Defects in intrinsic and innate immunity]]|B07=[[Auto-inflammatory disorders]]|B08=[[Complement deficiencies]]|B09=[[Phenocopies of primary immunodeficiency]] (PID)}} | ||
{{Family tree|!| | | |!| | | |!| | | |!| | | |!| | | |!| | | | | | | | | | | | | | | | |}} | {{Family tree|!| | | |!| | | |!| | | |!| | | |!| | | |!| | | | | | | | | | | | | | | | |}} | ||
{{Family tree|)| C01 |)| D01 |)| E01 |)| F01 |)| G01 |)| H01 | | | | | | | | | | | | | |C01=Severe combined<br>immunodeficiency (SCID)|D01=Combined immunodeficiency<br>with associated features|E01=Hypogammaglobulinemia|F01=Hemophagocytic lymphohistiocytosis (HLH)<br>& EBV susceptibility|G01=Congenital defects of<br>phagocyte number|H01=Bacterial and<br>parasitic infections}} | {{Family tree|)| C01 |)| D01 |)| E01 |)| F01 |)| G01 |)| H01 | | | | | | | | | | | | | |C01=Severe combined<br>immunodeficiency (SCID)|D01=Combined immunodeficiency<br>with associated features|E01=Hypogammaglobulinemia|F01=Hemophagocytic lymphohistiocytosis (HLH)<br>& EBV susceptibility|G01=Congenital defects of<br>phagocyte number|H01=Bacterial and<br>parasitic infections}} | ||
Revision as of 15:03, 29 October 2018
| Immunodeficiency | |
| ICD-10 | D84.9 |
|---|---|
| ICD-9 | 279.3 |
| DiseasesDB | 21506 |
| MeSH | D007153 |
|
Immunodeficiency Main Page |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Zahir Ali Shaikh, MD[2], Ali Akram, M.B.B.S.[3], Anmol Pitliya, M.B.B.S. M.D.[4]
Synonyms and keywords: Immune deficiency; immunity suppression; immunological deficiency; immunosuppression
Overview
Classification
| Immunodeficiency | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Immunodeficiency affecting cellular and humoral Immunity | Combined immunodeficiency | Predominantly antibody deficiency | Diseases of immune dysregulation | Congenital defects of phagocytes | Defects in intrinsic and innate immunity | Auto-inflammatory disorders | Complement deficiencies | Phenocopies of primary immunodeficiency (PID) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe combined immunodeficiency (SCID) | Combined immunodeficiency with associated features | Hypogammaglobulinemia | Hemophagocytic lymphohistiocytosis (HLH) & EBV susceptibility | Congenital defects of phagocyte number | Bacterial and parasitic infections | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Combined immunodeficiencies generally less pronounced than severe combined immunodeficiency | Combined immunodeficiency with syndromic features | Other antibody deficiencies | Syndromes with autoimmunity and others | Congenital defects of phagocyte function | Mendelian susceptibility to mycobacterial disease (MSMD) & viral infections | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
References
ca:Immunodeficiència de:Immundefekt el:Ανοσολογική ανεπάρκεια he:כשל חיסוני