Immunodeficiency: Difference between revisions
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==Classification== | ==Classification== | ||
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{{Family tree| | | | | | | | | | | | | | | | | A01 | | | | | | | | |A01=Immunodeficiency}} | {{Family tree| | | | | | | | | | | | | | | | | A01 | | | | | | | | |A01=Immunodeficiency}} | ||
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{{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|`| 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}} | ||
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==References== | ==References== | ||
Revision as of 14:28, 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-imflammatory 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