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{{CMG}}; {{AE}} {{Akram}}
{{CMG}}; {{AE}} {{Akram}}


==Overview==
== Classification ==
Immunodeficiency disorders are classified into two types:
* Primary immunodeficiency
* Secondary immunodeficiency
=== Primary immunodeficiency: ===
{| class="wikitable"
|+
!Primary immunodeficiency disorders
!
!
!
!
|-
|Phagocyte cell defects
|Decreased number
Functional Defects
|Schwachman-Diamond Syndrome
G6PC3 deficiency
Cohen Syndrome
Barth Syndrome
Glycogen Storage Disease Type 1b
Clericuzio Syndrome
VPS45 deficiency
P14/LAMTOR2 deficiency
JAGN1 deficiency
3-methylglutaconic aciduria
SMARCD2 deficiency
WDR1 deficiency
HYOU1 deficiency
Elastase deficiency
HAX1 deficiency(Kostmann Disease)
GFI1 deficiency
G-CSF receptor deficiency
X-linked neutropenia /mylodysplasia WAS GOF
Neutropenia with combined immune deficiency
Cystic Fibrosis
Papillion-Lefèvre
Localized juvenile peridontitis
B-Actin
Leukocyte adhesion deficiency
GATA2 def (MonoMac sd)
Specific granule deficiency
Pulmonary alveolar proteinosis
Chronic Granulomatous Disease
Rac 2 def
G6PD def Class 1
|
|
|-
|Defects in Intrinsic and Innate immunity
|Predisposition to bacterial infections
|
|
|
|-
|
|
|
|
|
|}
==Algorithms==
{{Family tree/start}}
{{Family tree | | | | | | | | | | A01 | | | | | | | | | | | | | | |A01=Immunodeficiency affecting cellular and humoral immunity}}
{{Family tree | | | | | |,|-|-|-|-|^|-|-|-|-|.| | | | | | | | | | |}}
{{Family tree | | | | | B01 | | | | | | | | B02 | | | | | | | | | |B01=CD19 NL: SCID T-ve B+ve|B02=CD19 ↓: SCID T-ve B-ve}}
{{Family tree | | |,|-|-|^|-|-|.| | | |,|-|-|^|-|-|.| | | | | | | |}}
{{Family tree | | C01 | | | | C02 | | C03 | | | | C04 | | | | | | |C01=SCID T-ve B+ve NK-ve|C02=SCID T-ve B+ve NK+ve|C03=SCID T-ve B-ve NK-ve|C04=SCID T-ve B-ve NK+ve}}
{{Family tree | |!| | | | | |!| | | |!| | | | | |,|^|-|-|-|.| | | |}}
{{Family tree | |)| D01 | | |)| E01 |)| F01 | | G01 | | | G02 | | |D01=yc deficiency|E01=IL7Ra .|F01=ADA def|G01=Microcephaly present|G02=Microcephaly absent}}
{{Family tree | |!| | | | | |!| | | |!| | | | |!| | | | |!| | | | |}}
{{Family tree | |`| D02 | | |)| E02 |`| F02 | |)| H01 | |)| H05 | |D02=JAK-3 def|E02=CD3D, CD3E, CD247|F02=Reticular dysgenesis|H01= DNA Ligase IV def|H05=RAG1/2 def}}
{{Family tree | | | | | | | |!| | | | | | | | |!| | | | |!| | | | |}}
{{Family tree | | | | | | | |)| E03 | | | | | |)| H02 | |`| H06 | |E03=CD45 def|H02=XLF def|H06=DCLRE1C def}}
{{Family tree | | | | | | | |!| | | | | | | | |!| | | | | | | | | |}}
{{Family tree | | | | | | | |)| E04 | | | | | |`| H03 | | | | | | |E04=Coronin-1A def|H03=DNA PKcs def}}
{{Family tree | | | | | | | |!| | | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | |`| E05 | | | | | | | | | | | | | | | |E05=Winged helix def}}
{{Family tree/end}}
==Combined Immunodeficiency Diseases with associated or syndromic features==
{{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|F04=CHARGE Syndrome|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}}
===Phenocopies of PID===
{{Family tree/start}}
{{Family tree | | | | | A01 | | | | |A01=Phenocopies of PID}}
{{Family tree | | |,|-|-|^|-|-|.| | |}}
{{Family tree | | B01 | | | | | B02 | | |B01=Associated with Somatic Mutations|B02=Associated with Auto-Antibodies}}
{{Family tree | |!| | | | | | |!| | | | |}}
{{Family tree | |)| C01 | | | |)| D01 | |C01=ALPS-SFAS|D01=Chronic mucocutaneous candidiasis}}
{{Family tree | |!| | | | | | |!| | | | |}}
{{Family tree | |)| C02 | | | |)| D02 | |C02=RALD(RAS-associated autoimmune leukoproliferative disease)|D02=Adult-onset immunodeficiency with susceptibility to mycobacteria}}
{{Family tree | |!| | | | | | |!| | | | |}}
{{Family tree | |)| C03 | | | |)| D03 | |C03=Cryopyrinopathy(Muckle-Wells Syndrome)|D03=Recurrentt skin infections}}
{{Family tree | |!| | | | | | |!| | | | | |}}
{{Family tree | |`| C04 | | | |)| D04 | | |C04=Hypereosinophilic syndrome due to somatic mutations in STAT5b|D04=Pulmonary alveolar proteinosis}}
{{Family tree | | | | | | | | |!| | | | | |}}
{{Family tree | | | | | | | | |)| D05 | | |D05=Acquired angiooedema}}
{{Family tree | | | | | | | | |!| | | | | |}}
{{Family tree | | | | | | | | |)| D06 | | |D06=Atypical Hemolytic Uremic Syndrome}}
{{Family tree | | | | | | | | |!| | | | | |}}
{{Family tree | | | | | | | | |`| D07 | | |D07=Thymoma with hypogammaglobulinemia}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}}
{{Family tree/end}}
===Predominantly Antibody deficiencies===
{{Family tree/start}}
{{Family tree | | | | | | | A01 | | |A01=Predominantly Antibody deficiencies, a: Hypogammaglobulinemia}}
{{Family tree | | | | | | | |!| | | |}}
{{Family tree | | | | | | | B01 | | |B01=Serum immunoglobulin assays : IgG, IgA, IgM, IgE}}
{{Family tree | | | | | | | |!| | | |}}
{{Family tree | | | | | | | C01 | |C01=IgG, IgA, and/or IgM ↓↓
→ B Lymphocyte (CD19+) enumeration (CMF)}}
{{Family tree | | |,|-|-|-|-|^|-|-|.| |}}
{{Family tree | | D01 | | | | | | D02 | |D01=B absent|D02= B >1%}}
{{Family tree | |!| | | | | |,|-|-|^|-|.| | |}}
{{Family tree | |)| E01 | | F01 | | | G01 | |E01=X-Linked Agammaglobulinemia|F01=Common Variable Immunodeficiency Phenotype|G01=CD19 deficiency}}
{{Family tree | |!| | | | |!| | | | | |!| | |}}
{{Family tree | |)| E02 | |)| F02 | | G02 | |E02=µ heavy chain Def|F02=CVID with no gene defect specified|G02=CD20 deficiency}}
{{Family tree | |!| | | | |!| | | | | |!| | |}}
{{Family tree | |)| E03 | |)| F03 | | G03 | |E03=Igα def|F03=PIK3CD mutation(GOF),PIK3R1 deficiency(LOF)|G03=CD21 deficiency}}
{{Family tree | |!| | | | |!| | | | | |!| |}}
{{Family tree | |)| E04 | |)| F04 | | G04 | | |E04=Igβ def|F04=PTEN deficiency(LOF)|G04=TRNT1 deficiency}}
{{Family tree | |!| | | | |!| | | | | |!| | |}}
{{Family tree | |)| E05 | |)| F05 | | G05 | |E05=BLNK def|F05=CD81 deficiency|G05=NFKB1 deficiency}}
{{Family tree | |!| | | | |!| | | | | |!| | |}}
{{Family tree | |)| E06 | |)| F06 | | G06 | | |E06=λ5 def|F06=TACI deficiency|G06=NFKB2 deficiency}}
{{Family tree | |!| | | | |!| | | | | |!| | |}}
{{Family tree | |)| E07 | |)| F07 | | G07 | |E07=PI3KR1 def|F07=BAFF receptor deficiency|G07=IKAROS deficiency}}
{{Family tree | |!| | | | |!| | | | | |!| | |}}
{{Family tree | |`| E08 | |)| F08 | | G08 | |E08=E47 transcription factor def|F08=TWEAK deficiency|G08=ATP6AP1 deficiency}}
{{Family tree | | | | | | |!| | | |}}
{{Family tree | | | | | | |)| F09 | |F09=Mannosyl-oligosaccharide glucosidase deficiency (MOGS)}}
{{Family tree | | | | | | |!| | | | |}}
{{Family tree | | | | | | |)| F10 | | |F10=TTC37 deficiency}}
{{Family tree | | | | | | |!| | |}}
{{Family tree | | | | | | |`| F11 | | |F11=IRF2BP2 deficiency}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}}
{{Family tree/end}}
{{Family tree/start}}
{{Family tree | | | | | | | | | | | | | | | | A01 | | | | | | | | | | | | | | | | | |A01=Predominantly Antibody deficiencies. b:Other antibody deficiencies}}
{{Family tree | | | | | | | | | | | | | | | | |!| | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | | | | | | | | | B01 | | | | | | | | | | | | | | | | | |B01=Serum Immunolobulin Assays: IgG, IgA, IgM, IgE}}
{{Family tree | | | | | | | | | |,|-|-|-|-|-|-|+|-|-|-|-|-|.| | | | | | | | | | |}}
{{Family tree | | | | | | | | | C01 | | | | | C02 | | | | C03 | | | | | | | | | | | | | | | |C01=Severe Reduction in Serum IgG and IgA with NI/elevated IgM and Normal Numbers of B cells: Hyper IgM Syndromes|C02=Isotype, Light Chain, or Functional Deficiencies with Generally NI Numbers of B cells|C03=High B cell numbers due to constitutive NF-kB activation}}
{{Family tree | | | | | | | | |!| | | | | | |!| | | | | |!| | | | | | | | | | | |}}
{{Family tree | | | | | | | | |)| D01 | | | |)| D02 | | |`| D03 | | | | | | | | | | |D01=AID deficiency|D02=Selective IgA deficiency|D03=CARD11 Gain of Function}}
{{Family tree | | | | | | | | |!| | | | | | |!| | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | |)| E01 | | | |)| E02 | | | | | | | | | | | | | | | | |E01=UNG deficiency|E02=Transient hypogammaglobuliemia of infancy}}
{{Family tree | | | | | | | | |!| | | | | | |!| | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | |)| F01 | | | |)| F02 | | | | | | | | | | | | | | | | |F01=INO80|F02=IgG subclass deficiency with IgA deficiency}}
{{Family tree | | | | | | | | |!| | | | | | |!| | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | |`| G01 | | | |)| G02 | | | | | | | | | | | | | | | | |G01=MSH6|G02=Isolated IgG subclass deficiency}}
{{Family tree | | | | | | | | | | | | | | | |!| | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | | | | | | | | |)| F03 | | | | | | | | | | | | | | | | |F03=Specific antibody deficiency with normal Ig levels and normal B cells}}
{{Family tree | | | | | | | | | | | | | | | |!| | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | | | | | | | | |)| G03 | | | | | | | | | | | | | | | |G03=Ig heavy chain muations and deletions}}
{{Family tree | | | | | | | | | | | | | | | |!| | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | | | | | | | | |)| H03 | | | | | | | | | | | | | | | |H03= Kappa chain deficiency}}
{{Family tree | | | | | | | | | | | | | | | |!| | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | | | | | | | | |`| I03 | | | | | | | | | | | | | | | |I03=Selective IgM deficiency}}
{{Family tree/end}}
===Congenital defects of phagocyte number===
{{Family tree/start}}
{{Family tree | | | | | A01 | | | | | |A01=Congenital defects of phagocyte number}}
{{Family tree | | |,|-|-|^|-|-|.| | | | |}}
{{Family tree | | B01 | | | | B02 | | | |B01=Syndrome associated|B02=No syndrome associated}}
{{Family tree | |!| | | | | |!| | | | |}}
{{Family tree | |)| C01 | | |)| D01 | | | | |C01=Shwachman-Diamond syndrome|D01=Elastase deficiency (SCN1)}}
{{Family tree | |!| | | | | |!| | | | |}}
{{Family tree | |)| C02 | | |)| D02 | | | |C02=G6PC3 deficiency (SCN4)|D02=HAX1 deficiency (Kostmann Disease) (SCN3)}}
{{Family tree | |!| | | | | |!| | | | |}}
{{Family tree | |)| C03 | | |)| D03 | | |C03=Glycogen storage disease type 1b|D03=GFI 1 deficiency (SCN2)}}
{{Family tree | |!| | | | | |!| | | |}}
{{Family tree | |)| C04 | | |)| D04 | |C04=Cohen syndrome|D04=X-linked neutropenia/myelodysplasia WAS GOF}}
{{Family tree | |!| | | | | |!| | |}}
{{Family tree | |)| C05 | | |)| D05 | |C05=Barth Syndrome|D05=G-CSF receptor deficiency}}
{{Family tree | |!| | | | | |!| | |}}
{{Family tree | |)| C06 | | |`| D06 | |C06=Clericuzio syndrome (poikiloderma with neutropenia)|D06=Neutropenia with combined immune deficiency}}
{{Family tree | |!| | | | |}}
{{Family tree | |)| C07 | | | |C07=VPS45 deficiency(SCN5)}}
{{Family tree | |!| | | |}}
{{Family tree | |)| C08 | | | |C08=P14/LAMTOR2 deficiency}}
{{Family tree | |!| | | |}}
{{Family tree | |)| C09 | | | |C09=JAGN1 deficiency}}
{{Family tree | |!| | | | | | |}}
{{Family tree | |)| C10 | | | | |C10=methylglutacoic aciduria}}
{{Family tree | |!| | | | |}}
{{Family tree | |)| C11 | | | | |C11=SMARCD2 deficiency}}
{{Family tree | |!| | | | |}}
{{Family tree | |)| C12 | | | | |C12=WDR1 deficiency}}
{{Family tree | |!| | | | |}}
{{Family tree | |`| C13 | | | |C13=HYOU1 deficiency}}
{{Family tree/end}}
===Congenital defects of phagocyte function===
{{Family tree/start}}
{{Family tree | | | | | | | A01 | | | | | | | | | | | | | | | | | | |A01=Congenital defects of phagocyte function}}
{{Family tree | | | |,|-|-|-|^|-|-|-|.| | | | | | | | | | |}}
{{Family tree | | | B01 | | | | | | B02 | | | | | | | | | | |B01=Syndrome associated|B02=No Syndrome associated;DHR assay(or NBT test)?}}
{{Family tree | | |!| | | | | | |,|-|^|-|-|.| | | | |}}
{{Family tree | | |)| C01 | | | C02 | | | C03 | | | | | |C01=Cystic Fibrosis|C02=Normal|C03=Abnormal}}
{{Family tree | | |!| | | | | |!| | | | |!| | | | |}}
{{Family tree | | |)| D01 | | |)| D02 | |)| D03 | | | | | | |D01=Papillion-Lefèvre|D02=GATA2 def (MonoMac syndrome|D03=CGD}}
{{Family tree | | |!| | | | | |!| | | | |!| | | | | |}}
{{Family tree | | |)| E01 | | |)| E02 | |)| E03 | | | | | | |E01=Localized juvenile periodontitis|E02=Specific granule deficiency|E03=Rac 2 deficiency}}
{{Family tree | | |!| | | | | |!| | | | |!| | | | | |}}
{{Family tree | | |)| F01 | | |`| F02 | |`| F03 | | | | | | |F01=B-Actin|F02=Pulmonary alveolar proteinosis|F03=G6PD def Class 1}}
{{Family tree | | |!| | | | | | | | | | | | | | | | | | | | | | | | | |}}
{{Family tree | | |`| G01 | | | | | | | | | | | | | | | | | | | | | | | | |G01=Leukocyte adhesion deficiency}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}}
{{Family tree/end}}
===Auto-inflammatory disorders===
{{Family tree/start}}
{{Family tree | | | | | | | | | | | | | | | | | | | A01 | | | | | | | | | | | | | | | | | | | |A01=Auto-inflammatory disorders}}
{{Family tree | | | | | | | | | | | | | | | | | | | |!| | | | | | | | | | | | | |}}
{{Family tree | | | | | | | |,|-|-|-|-|-|v|-|-|-|-|-|+|-|-|-|-|-|-|v|-|-|-|-|-|-|-|.| |}}
{{Family tree | | | | | | | |!| | | | | |!| | | | | |!| | | | | | |!| | | | | | | |!| | |}}
{{Family tree | | | | | | | B01 | | | | B02 | | | | B03 | | | | | B04 | | | | | | B05 | | | | | | |B01=Recurrent inflammation|B02=Systemic inflammation with urticaria rash|B03=Others|B04=Sterile inflammation (skin/bone/joints)|B05=Type 1 Interferonopathies}}
{{Family tree | | | | | | |!| | | | | |!| | | | | |!| | | | | |,|-|^|-|-|.| | | |!| | | |}}
{{Family tree | | | | | | |)| C01 | | |)| D01 | | |)| E01 | | F01 | | | G01 | | |)| H01 | | | | | | | |C01=Familial Mediterranean Fever|D01=Familial Cold Autoinflammatory Syndrome (CAPS)|E01=CANDLE syndrome|F01=Predominant on the bone/joints|G01=Predominant on the skin|H01=Aicardi-Goutieres syndrome}}
{{Family tree | | | | | | |!| | | | | |!| | | | | |!| | | | |!| | | | |!| | | | |!| | | | | |}}
{{Family tree | | | | | | |)| C02 | | |)| D02 | | |)| E02 | |)| F02 | |)| G02 | |)| H02 | | | | | | |C02=Mevalonate kinase deficiency|D02=Muckle Wells syndrome|E02=COPA defect|F02=Pyogenic sterile arthritis, pyoderma gangrenosum, acne(PAPA) syndrome, hyperzincemia and hypercalprotectinemia|G02=Blau syndrome|H02=Spondyloenchondro-dysplasia with immune dysregulation}}
{{Family tree | | | | | | |!| | | | | |!| | | | | |!| | | | |!| | | | |!| | | | |!| | | |}}
{{Family tree | | | | | | |`| C03 | | |)| D03 | | |`| E03 | |)| F03 | |)| G03 | |)| H03 | | | | | | | |C03=TNF receptor-associated periodic syndrome; TRAPS|D03=Neonatal onset multisystem inflammatory disease|E03=NLRC4-MAS(Macrophage activating syndrome)|F03=Chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anemia|G03=CAMPS|H03=STING-associated vasculopathy, infantile onset}}
{{Family tree | | | | | | | | | | | | |!| | | | | | | | | | |!| | | | |!| | | | |!| | | |}}
{{Family tree | | | | | | | | | | | | |)| D04 | | | | | | | |)| F04 | |)| G04 | |)| H04 | | | |D04=PLAID (PLCg2 associated antibody deficiency and immune dysregulation), or APLAID|F04=DIRA (Deficiency of the interleukin 1 receptor antagonist)|G04=DITRA|H04=ADA2 deficiency}}
{{Family tree | | | | | | | | | | | | |!| | | | | | | | | | |!| | | | |!| | | | |!| | | |}}
{{Family tree | | | | | | | | | | | | |)| D05 | | | | | | | |`| F05 | |)| G05 | |)| H05 | | | |D05=NLRP1 deficiency|F05=Cherubism|G05=ADAM17 deficiency|H05=XL reticulate pigmentary disorder}}
{{Family tree | | | | | | | | | | | | |!| | | | | | | | | | | | | | | |!| | | | |!| | | |}}
{{Family tree | | | | | | | | | | | | |`| D06 | | | | | | | | | | | | |)| G06 | |`| H06 | | | |D06=A20 haploinsufficiency|G06=SLC29A3 mutation|H06=USP18 deficiency}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | |!| | | | | | |}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | |)| G07 | | | | |G07=Otulipenia/ORAS}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | |!| | | | | |}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | |`| G08 | | | | |G08=AP153 deficiency}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}}
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}}
{{Family tree/end}}





Revision as of 00:56, 24 January 2019


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ali Akram, M.B.B.S.[2]



Diseases History and Symptoms Physical Examination Laboratory Findings Other Findings
Abdominal Pain Rectal Bleeding Fatigue Abdominal Tenderness Hyperpigmentation Anemia Gene(s) Gastrointestinal Tumors Cancers
Hereditary Non–Polyposis Colon Cancer + + +/– +
Carney Syndrome
Familial Adenomatous Polyposis + + + +/– +
Peutz–Jeghers syndrome + + + + + +
  • Breast
  • Lung
  • Pancreas
  • Ovaries
  • Sertoli cells
  • Uterine
Juvenile Polyposis Syndrome + +
Cowden Syndrome
  • Trichilemmoma
  • Skin hamartoma
  • Hyperplastic polyp
  • Macrocephaly
  • Breast fibrosis
Differential Diagnosis Similar Features Differentiating Features
Familial adenomatous polyposis
  • Familial inheritance, increased risk of colorectal cancer, extra-colonic tumors, and genetic mutations
  • Autosomal recessive, 100+ polyps and age under 40, centinel tumors are differently located than hereditary nonpolyposis colorectal cancer, such as: multiple osteomas, dental anomalies, congenital hypertrophy of the retinal pigment epithelium (CHRPE), and APC is the gene affected
Juvenile polyposis
  • Familial inheritance, autosomal dominant, increased risk of colorectal cancer, extra-colonic tumors, and genetic mutations
  • Gastrointestinal hamartomatous polyps, on physical exam lip pigmentation is common, and STK11 is the gene affected
Cowden syndrome
  • Familial inheritance, rare autosomal dominant, increased risk of colorectal cancer, and genetic mutations
  • Intestinal hamartomatous polyps, physical exam may show macrocephaly, and PTEN is the gene affected

=References