Immunodeficiency: Difference between revisions
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{{CMG}} | {{CMG}} {{shyam}}; {{AE}} {{Anmol}}, {{Akram}}, {{ZAS}} , {{Sali}}, {{Sab}} | ||
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{{SK}} Immune deficiency; immunity suppression; immunological deficiency; immunosuppression | |||
==Overview== | |||
Immunodeficiency can be caused by a variety of conditions including autoimmunity, infections, congenital defects, complement defects, or auto-inflammatory states. | |||
[[ | ==Classification== | ||
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[[ | {{Family tree| | | | | | | | | | | | | | | | | A01 | | | | | | | | |A01=Immunodeficiency}} | ||
[[ | {{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-inflammatory disorders]]|B08=[[Complement deficiencies]]|B09=[[Phenocopies of primary immunodeficiency]] (PID)}} | ||
{{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|!| | | |!| | | |!| | | |!| | | |!| | | |!| | | | | | | | | | | | | | | | |}} | |||
{{Family tree|`| C02 |`| D02 |`| E02 |`| F02 |`| G02 |`| H02 | | | | | | | | | | | | | |C02=Combined immunodeficiencies<br>generally less pronounced than<br>severe combined immunodeficiency|D02=Combined immunodeficiency<br>with syndromic features|E02=Other antibody<br>deficiencies|F02= Syndromes with<br>autoimmunity and others|G02=Congenital defects of<br>phagocyte function|H02=Mendelian susceptibility to<br>mycobacterial disease (MSMD)<br>& viral infections}} | |||
{{Family tree/end}} | |||
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==References== | |||
{{Reflist|2}} | |||
[[Category:Hematology]] | |||
[[Category:Medicine]] | |||
[[Category:Immunology]] | |||
[[Category: | [[Category:Up-To-Date]] | ||
[[Category: |
Latest revision as of 22:21, 29 July 2020
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] Shyam Patel [2]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[3], Ali Akram, M.B.B.S.[4], Zahir Ali Shaikh, MD[5] , Syed Musadiq Ali M.B.B.S.[6], Sabawoon Mirwais, M.B.B.S, M.D.[7]
Synonyms and keywords: Immune deficiency; immunity suppression; immunological deficiency; immunosuppression
Overview
Immunodeficiency can be caused by a variety of conditions including autoimmunity, infections, congenital defects, complement defects, or auto-inflammatory states.
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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||