|
|
| Line 29: |
Line 29: |
|
| |
|
| ===Combined Immunodeficiency=== | | ===Combined Immunodeficiency=== |
| {{Family tree/start}}
| |
| {{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | A01 | | | | | | | | | |A01=Combined Immunodeficiency Diseases with associated or syndromic features}}
| |
| {{Family tree | | | |,|-|-|-|-|-|-|v|-|-|-|-|-|v|-|-|-|-|-|v|-|-|-|-|+|-|-|-|-|v|-|-|-|-|v|-|-|-|-|v|-|-|-|-|.| |}}
| |
| {{Family tree | | | B01 | | | | | B02 | | | | B03 | | | | B04 | | | B05 | | | B06 | | | B07 | | | B08 | | | B09 | | | | | | | | | | | | | |B01=Congenital thromocytopenia|B02=DNA Repair Defects|B03=Immuno-osseous dysplasias|B04=Thymic Defects with additional congenital anomalies|B05=Hyper-IgE syndromes(HIES)|B06=Dyskeratosis congenita (DKC)|B07=Defects of Vitamin B12 and Folate metabolism|B08=Anhidrotic Ectodermodysplasia with ID|B09=Others}}
| |
| {{Family tree | | |!| | | | | | |!| | | | | |!| | | | | |!| | | | |!| | | | |!| | | | |!| | | | |!| | | | |!| | | | | | |}}
| |
| {{Family tree | | |)| C01 | | | |)| D01 | | |)| E01 | | |)| F01 | |)| G01 | |)| H01 | |)| I01 | |)| J01 | |)| K01 | | | | | | |C01=Wiskott Aldrich Syndrome|D01=Ataxia telangiectasia|E01=Cartilage Hair Hypoplasia|F01=DiDeorge Syndrome|G01=Job Syndrome|H01=Dyskeratosis congenita|I01=Transcobalmin 2 deficiency|J01=NEMO deficiency|K01=Purine nucleoside phosphorylase deficiency}}
| |
| {{Family tree | | |!| | | | | | |!| | | | | |!| | | | | |!| | | | |!| | | | |!| | | | |!| | | | |!| | | | |!| | | | | | | | }}
| |
| {{Family tree | | |)| C02 | | | |)| D02 | | |)| E02 | | |)| F02 | |)| G02 | |)| H02 | |)| I02 | |`| J02 | |)| K02 | | | | | | | |C02=XL thrombocytopenia|D02=Nijmegen breakage Syndrome|E02=Schimke Syndrome|F02=TBX1 deficiency|G02=Comel Netherton Syndrome|H02= COATS plus syndrome|I02=Deficiency causing hereditary folate malabsorption|J02=EDA-ID due to IKBA GOF mutation|K02=ID with multiple intestinal atresias}}
| |
| {{Family tree | | |!| | | | | | |!| | | | | |!| | | | | |!| | | | |!| | | | |!| | | | |!| | | | | | | | | |!| | | | | | | | | }}
| |
| {{Family tree | | |)| C03 | | | |)| D03 | | |)| E03 | | |)| F03 | |`| G03 | |)| H03 | |`| I03 | | | | | | |)| K03 | | | | | | | | |C03=WIP deficiency|D03=Bloom syndrome|E03=MYSM1 deficiency|F03=Chromosome 10p13-p14 deletion Syndrome|G03=PGM3 deficiency|H03=SAMD9|I03=Methylene-tetrahydrofolate-dehydrogenase 1 deficiency|K03=Hepatic veno-occlusive disease with immunodeficiency}}
| |
| {{Family tree | | |!| | | | | | |!| | | | | |!| | | | | |!| | | | | | | | | |!| | | | | | | | | | | | | | |!| | | | | | | | | | | }}
| |
| {{Family tree | | |`| C04 | | | |)| D04 | | |)| E04 | | |`| F04 | | | | | | |`| H04 | | | | | | | | | | | |)| K04 | | | | | | | | | |C04=ARPC1B deficiency|D04=PMS2 deficiency|E04=MOPD1 deficiency|H04=SAMD9L|K04=Vici Syndrome}}
| |
| {{Family tree | | | | | | | | | |!| | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |!| | | | | | |}}
| |
| {{Family tree | | | | | | | | | |)| D05 | | |`| E05 | | | | | | | | | | | | | | | | | | | | | | | | | | | |)| K05| | | | | | |D05=Immunodeficiency with centromeric instability and facial anomalies(ICF1, ICF2, ICF3, ICF4)|E05=EXTL3 deficiency|K05=HOIL1 deficiency, HOIP1 deficiency}}
| |
| {{Family tree | | | | | | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |!| | | | |}}
| |
| {{Family tree | | | | | | | | | |)| D06 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |)| K06 | | | | |D06=MCM4 deficiency|K06=Calcium Channel Defects(ORAI-1 deficiency, STIM1 deficiency)}}
| |
| {{Family tree | | | | | | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |!| | | | | | |}}
| |
| {{Family tree | | | | | | | | | |)| D07 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |)| K07 | | | | | | |D07=RNF168 deficiency|K07=Hennekam-lymphangiectasia-lymphedema syndrome}}
| |
| {{Family tree | | | | | | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |!| | | | | | | |}}
| |
| {{Family tree | | | | | | | | | |)| D08 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |)| K08 | | | | | | |D08=POLE1 deficiency|K08=STAT5b deficiency}}
| |
| {{Family tree | | | | | | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |!| | | | | | | |}}
| |
| {{Family tree | | | | | | | | | |)| D09 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |`| K09 | | | | | | |D09=POLE2 deficiency|K09=Kabuki Syndrome}}
| |
| {{Family tree | | | | | | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}}
| |
| {{Family tree | | | | | | | | | |)| D10 | | | | | | | | | | | | | | | | | | | | | | | |D10=NSMCE3 deficiency}}
| |
| {{Family tree | | | | | | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | |}}
| |
| {{Family tree | | | | | | | | | |)| D11 | | | | | | | | | | | | | | | | | | | | | | | |D11=ERCC6L2(Hebo deficiency)}}
| |
| {{Family tree | | | | | | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | |}}
| |
| {{Family tree | | | | | | | | | |)| D12 | | | | | | | | | | | | | | | | | | | | | | | |D12=Ligase 1 deficiency}}
| |
| {{Family tree | | | | | | | | | |!| | | | | | | | | | | | | | | | | | | | | | | | |}}
| |
| {{Family tree | | | | | | | | | |`| D13 | | | | | | | | | | | | | | | | | | | | | | | |D13=GINS1 deficiency}}
| |
| {{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}}
| |
| {{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}}
| |
| {{Family tree/end}}
| |
|
| |
|
| ===Diseases of Immune Dysregulation=== | | ===Diseases of Immune Dysregulation=== |
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) | |
|
Immunodeficiency Affecting Cellular and Humoral Immunity
Combined Immunodeficiency
Diseases of Immune Dysregulation
Congenital Defects of Phagocytes
Defects in Intrinsic and Innate Immunity
Auto-imflammatory Disorders
Complement Deficiencies
Phenocopies of Primary Immunodeficiency (PID)
References
ca:Immunodeficiència
de:Immundefekt
el:Ανοσολογική ανεπάρκεια
he:כשל חיסוני
Template:WH
Template:WS