| Combined B and T cell immunodeficiencies | |||
| T-B- Severe combined immunodeficiency (SCID) | |||
| Disease | Fact file | Gene | Animal models |
| Reticular dysgenesis | 1 | ||
| RAG1 deficiency | 2 | RAG1 | Mus musculus (Mouse): |
| RAG2 deficiency | 3 | RAG2 | Mus musculus (Mouse): |
| Omenn syndrome | 4 | RAG1 | Mus musculus (Mouse): Mus musculus (Mouse): |
| Artemis deficiency | 5 | DCLRE1C | FlyBase:: |
| T-B+ SCID | |||
| Disease | Fact file | Gene | Animal models |
| X-linked SCID(γc-chain deficiency) | 8 | IL2RG | M. musculus:: FlyBase:: |
| JAK3 deficiency | 9 | JAK3 | Mouse:: FlyBase:: |
| Interleukin 7 receptor deficiency | 106 | IL7R | Mouse: Rat: |
| CD45 deficiency | 6 | PTPRC | Mouse: Fly: C. elegans: |
| CD3delta deficiency | 111 | CD3D | Mouse: Rat: |
| T-cell immunodeficiency, congenital alopecia, and nail dystrophy | 128 | FOXN1 | Mouse: |
| Deficiencies of purine metabolism | |||
| Disease | Fact file | Gene | Animal models |
| Adenosine deaminase deficiency | 10 | ADA | Mouse:: |
| Purine nucleoside phosphorylase deficiency | 11 | NP | Mouse: FlyBase: C. elegans: |
| Major histocompatibility complex class II deficiency | |||
| Disease | Fact file | Gene | Animal models |
| CIITA, MHCII transactivating protein deficiency | 12 | CIITA | Mouse: Fly: C. elegans: |
| RFX-5, MHCII promoter X box regulatory factor 5 deficiency | 13 | RFX5 | Mouse: Fly: C. elegans: |
| Regulatory factor X-associated protein deficiency | 14 | RFXAP | Fly: C. elegans: |
| RFXANK, Ankyrin repeat containing regulatory factor X-associated protein deficiency | 15 | RFXANK | Mouse: Fly: C. elegans: |
| Major histocompatibility complex class I deficiency | |||
| Disease | Fact file | Gene | Animal models |
| TAP2 deficiency | 60 | TAP2 | |
| TAP1 deficiency | 107 | TAP1 | Mouse: Rat: |
| Tapasin deficiency | 136 | TAPBP | Mouse: Rat: |
| Hyper-IgM syndrome | |||
| Disease | Fact file | Gene | Animal models |
| X-linked hyper-IgM syndrome (CD40L deficiency) | 16 | TNFSF5 | Mus musculus (Mouse): |
| CD40 deficiency | 18 | CD40 | |
| CD3 deficiency | |||
| Disease | Fact file | Gene | Animal models |
| CD3ε deficiency | 20 | CD3E | Mouse: Fly: C. elegans: |
| CD3γ deficiency | 21 | CD3G | Mouse: Fly: C. elegans: |
| CD3Zeta deficiency | 149 | CD247 | Mouse: |
| Other | |||
| Disease | Fact file | Gene | Animal models |
| ZAP-70 deficiency | 62 | ZAP70 | |
| IL-2 receptor α-chain deficiency (CD25 deficiency) | 63 | IL2RA | |
| CD8α deficiency | 64 | CD8A | |
| p56 Lck deficiency | 137 | LCK | Mouse: Rat: |
| Schimke immuno-osseous dysplasia | 148 | SMARCAL1 | Mouse: |
| Cernunnos deficiency | 152 | NHEJ1 | Mouse: |
| TMEM142 deficiency | 147 | ORAI1 | |
| Deficiencies predominantly affecting antibody production | |||
| Agammaglobulinemia | |||
| Disease | Fact file | Gene | Animal models |
| X-linked agammaglobulinemia | 22 | BTK | Mouse: |
| X-linked hypogammaglobulinemia with growth hormone deficiency | 23 | ||
| BLNK deficiency | 24 | BLNK | Mouse: Fly: C. elegans: |
| Igα deficiency | 25 | CD79A | |
| μ heavy-chain deficiency | 26 | IGHM | Mouse: Fly: |
| λ5 surrogate light-chain deficiency | 27 | IGLL1 | Mouse: C. elegans: |
| Non-Bruton type autosomal dominant agammaglobulinemia | 151 | LRRC8A | Mouse: |
| Igβ deficiency | 159 | CD79B | Mouse: |
| Light-chain deficiency | |||
| Disease | Fact file | Gene | Animal models |
| κ light-chain deficiency | 65 | IGKC | Mouse: R.norvegicus : |
| Selective deficiency of IgG subclass, IgE and/or IgA class or subclass | |||
| Disease | Fact file | Gene | Animal models |
| γ1 isotype deficiency | 28 | IGHG1 | Mouse: Fly: |
| γ2 isotype deficiency | 29 | IGHG2 | Fly: |
| Partial γ3 isotype deficiency | 30 | IGHG3 | Fly: |
| γ4 isotype deficiency | 31 | IGHG4 | Fly: |
| α1 isotype deficiency | 32 | IGHA1 | Fly: |
| α2 isotype deficiency | 33 | IGHA2 | Fly: |
| ε isotype deficiency | 34 | IGHE | Mouse: Fly: |
| IgG subclass deficiency with or without IgA deficiency | 35 | ||
| IgA deficiency | 67 | IGAD1 | |
| Common variable immunodeficiency | |||
| Disease | Fact file | Gene | Animal models |
| Common variable immunodeficiency of unknown origin | 66 | ||
| ICOS deficiency | 116 | ICOS | Mouse: |
| TNFRSF13B deficiency | 153 | TNFRSF13B | Mouse: |
| Other antibody deficiencies | |||
| Disease | Fact file | Gene | Animal models |
| Antibody deficiency with normal immunoglobulin levels | 68 | ||
| Transient hypogammaglobulinemia of infancy | 69 | ||
| CD19 deficiency | 150 | CD19 | Mouse: |
| Defects of class-switch recombination and somatic hypermutation (Hyper-IgM syndromes) affecting B cells | |||
| Disease | Fact file | Gene | Animal models |
| AID deficiency | 17 | AICDA | Mouse: Fly: C.elegans: |
| UNG deficiency | 127 | UNG | Mouse: |
| Selective deficiency in Ig class-switch recombination | 138 | ||
| Defects in lymphocyte apoptosis | |||
| Autoimmune lymphoproliferative syndrome | |||
| Disease | Fact file | Gene | Animal models |
| Autoimmune lymphoproliferative syndrome, type Ia | 36 | TNFRSF6 | Mouse: Fly: |
| Autoimmune lymphoproliferative syndrome, type 1B | 37 | FASLG | Mouse: Fly: |
| Autoimmune lymphoproliferative syndrome type II | 109 | CASP10 | Mouse: |
| Autoimmune lymphoproliferative syndrome type IIB | 110 | CASP8 | Mouse: Rat: |
| ALPS type III | 162 | NRAS | Mouse: |
| Other well-defined immunodeficiency syndromes | |||
| Wiskott-Aldrich syndrome and X-linked thrombocytopenia | 71 | WAS | |
| Autoimmune disorders | |||
| Disease | Fact file | Gene | Animal models |
| Autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy | 72 | AIRE | |
| X-linked immunodeficiency, polyendocrinopathy, enteropathy(IPEX) | 78 | FOXP3 | |
| X-linked lymphoproliferative disease (Duncan disease) | 73 | SH2D1A | |
| DiGeorge-anomaly | 74 | DGCR | |
| Hyper-IgE recurrent infection syndrome | 75 | TYK2 | Mouse: Mouse: |
| Chronic mucocutaneous candidiasis | 76 | ||
| Cartilage-hair hypoplasia | 77 | RMRP | |
| Epidermodysplasia verruciformis | |||
| Disease | Fact file | Gene | Animal models |
| Epidermodysplasia verruciformis type 1 | 114 | TMC6 | Mouse: |
| Epidermodysplasia verruciformis type 2 | 115 | TMC8 | Mouse: |
| Netherton syndrome | 133 | SPINK5 | Mouse: Rat: |
| Natural killer deficiency | 135 | FCGR3A | Mouse: Rat: |
| Transcobalamin II deficiency | 130 | TCN2 | Mouse: Rat: |
| Osteopetrosis, AR | 157 | TCIRG1 | Mouse: |
| Hepatic veno-oclussive disease with immunodeficiency syndrome | 158 | SP110 | |
| Tyk2 deficiency | 163 | TYK2 | Mouse: |
| X-linked lymphoproliferative syndrome 2 | 165 | BIRC4 | Mouse: |
| STAT3 deficiency | 167 | STAT3 | Mouse: |
| Defects of phagocyte function | |||
| Chronic granulomatous disease | |||
| Disease | Fact file | Gene | Animal models |
| X-linked chronic granulomatous disease | 38 | CYBB | Mouse: C. elegans: |
| p22phox deficiency | 39 | CYBA | Mouse: Fly: C. elegans: |
| p47phox deficiency | 40 | NCF1 | Mouse: Fly: C. elegans: |
| p67phox deficiency | 41 | NCF2 | Mouse: Fly: C. elegans: |
| Leukocyte adhesion defects | |||
| Disease | Fact file | Gene | Animal models |
| Leukocyte adhesion deficiency I | 42 | ITGB2 | Mouse: Fly: C. elegans: |
| Leukocyte adhesion deficiency II | 43 | SLC35C1 | |
| LAD3 deficiency | 139 | RASGRP2 | Mouse: |
| LAD with RAC2 deficiency | 123 | RAC2 | Mouse: |
| Chediak-Higashi syndrome | 79 | LYST | |
| Griscelli syndrome | |||
| Disease | Fact file | Gene | Animal models |
| Griscelli syndrome, type 1 | 80 | MYO5A | |
| Griscelli syndrome, type 2 | 122 | RAB27A | Mouse: |
| Griscelli syndrome, type 3 | 156 | MLPH | Mouse: |
| Glucose 6-phosphate dehydrogenase deficiency | 81 | G6PD | |
| Myeloperoxidase deficiency | 82 | MPO | |
| Glycogen storage disease Ib | 83 | G6PC | |
| Shwachman syndrome | 84 | SBDS | Mouse: |
| Neutropenia | |||
| Disease | Fact file | Gene | Animal models |
| Severe congenital neutropenias, including Kostmann syndrome | 85 | CSF3R | Mouse: |
| Cyclic neutropenia | 86 | ELA2 | Mouse: |
| GFI1 deficiency | 129 | GFI1 | Mouse: |
| Familial haemophagocytic lymphohistiocytosis | |||
| Disease | Fact file | Gene | Animal models |
| Familial haemophagocytic lymphohistiocytosis type 1 | 104 | ||
| Familial haemophagocytic lymphohistiocytosis type 2 | 105 | PRF1 | |
| Familial hemophagocytic lymphohistiocytosis 3 | 126 | UNC13D | Mouse: |
| Familial haemophagocytic lymphohistiocytosis type 4 | 155 | STX11 | Mouse: |
| Hoyeraal-Hreidarsson syndrome/Dyskeratosis congenita | 113 | DKC1 | Mouse: |
| CD64 deficiency | 132 | FCGR1A | Mouse: Rat: |
| Hermansky-Pudlak syndrome 2 | 108 | AP3B1 | Mouse: Rat: |
| Barth syndrome | 134 | TAZ | Mouse: |
| Neutrophil-specific granule deficiency | 112 | CEBPE | Mouse: Rat: |
| Papillon-Lefevre syndrome | 154 | CTSC | Mouse: |
| Disorders of pigmentation and immunodeficiency | |||
| Disease | Fact file | Gene | Animal models |
| p14 deficiency | 161 | MAPBPIP | Mouse: |
| Defects of innate immune system, receptors and signaling components | |||
| Interferon-γ (IFNγ) receptor deficiency | |||
| Disease | Fact file | Gene | Animal models |
| IFNγ1-receptor deficiency | 44 | IFNGR1 | Mouse: Fly: |
| IFNγ2-receptor deficiency | 45 | IFNGR2 | Mouse: Fly: |
| Interleukin-12 receptor β1 deficiency | 47 | IL12RB1 | Mouse: Fly: |
| Interleukin-12 (IL-12) p40 deficiency | 46 | IL12B | Mouse: Fly: |
| STAT1 deficiency | 70 | STAT1 | Mouse: |
| STAT5b deficiency | 125 | STAT5B | Mouse: |
| IRAK4 deficiency | 117 | IRAK4 | Mouse: |
| Autosomal dominant anhidrotic ectodermal dysplasia and T-cell immunodeficiency | 121 | NFKBIA | Mouse: Rat: |
| WHIM syndrome | 7 | CXCR4 | |
| X-linked hyper-IgM syndrome and hypohydrotic ectodermal dysplasia (Nemo deficiency) | 19 | IKBKG | Mouse: Fly: |
| UNC93B deficiency | 164 | UNC93B1 | Mouse: |
| TLR3 deficiency | 166 | TLR3 | Mouse: |
| DNA breakage associated syndromes and DNA epigenetic modification syndromes | |||
| DNA-breakage-associated syndromes | |||
| Disease | Fact file | Gene | Animal models |
| Ataxia-telengiectasia | 87 | ATM | |
| Nijmegen-breakage syndrome | 88 | NBS1 | |
| Ataxia-telangiectasia-like disorder | 120 | MRE11A | Mouse: |
| DNA ligase deficiency | |||
| Disease | Fact file | Gene | Animal models |
| DNA ligase I deficiency | 131 | LIG1 | Mouse: |
| DNA ligase deficiency IV | 118 | LIG4 | Mouse: |
| Bloom syndrome | 89 | BLM | |
| Immunodeficiency, centromere instability and facial abnormalities syndrome (ICF) | 124 | DNMT3B | Mouse: |
| Defects of the classical complement cascade proteins | |||
| C1q deficiency | |||
| Disease | Fact file | Gene | Animal models |
| C1q α-polypeptide deficiency | 48 | C1QA | Mouse: Fly: C. elegans: |
| C1q β-polypeptide deficiency | 49 | C1QB | Mouse: Fly: C. elegans: |
| C1q γ-polypeptide deficiency | 50 | C1QC | Mouse: Fly: C. elegans: |
| C1r and C1s deficiency | |||
| Disease | Fact file | Gene | Animal models |
| C1r deficiency | 51 | C1R | Mouse: Fly: C. elegans: |
| C1s deficiency | 52 | C1S | Fly: C. elegans: |
| C2 deficiency | 90 | C2 | |
| C3 deficiency | 61 | C3 | |
| C4 deficiency | |||
| Disease | Fact file | Gene | Animal models |
| C4A deficiency | 53 | C4A | Mouse: Fly: C. elegans: |
| C4B deficiency | 54 | C4B | Mouse: Fly: C. elegans: |
| C5 deficiency | 91 | C5 | |
| C6 deficiency | 92 | C6 | |
| C7 deficiency | 93 | C7 | |
| C8 deficiency | |||
| Disease | Fact file | Gene | Animal models |
| C8 α-polypeptide deficiency | 55 | C8A | Fly: C. elegans: |
| C8 β-polypeptide deficiency | 56 | C8B | Mouse: Fly: C. elegans: |
| C8 γ-polypeptide deficiency | 57 | C8G | Mouse: Fly: C. elegans: |
| C9 deficiency | 94 | C9 | |
| Defects of the alternative complement pathway | |||
| Factor B deficiency | 95 | BF | |
| Factor D deficiency | 98 | CFD | |
| Factor H1 deficiency | 101 | CFH | |
| Properdin factor C deficiency | 100 | CFP | |
| Defects of complement regulatory proteins | |||
| Hereditary angioedema | |||
| Disease | Fact file | Gene | Animal models |
| Hereditary angioedema | 97 | SERPING1 | |
| C4-binding protein deficiency | |||
| Disease | Fact file | Gene | Animal models |
| C4 binding protein α deficiency | 58 | C4BPA | Mouse: Fly: C. elegans: |
| C4 binding protein β deficiency | 59 | C4BPB | Mouse: Fly: C. elegans: |
| Hereditary angioedema type III | 160 | F12 | Mouse: |
| Decay-accelerating factor (CD55) deficiency | 102 | CD55 | |
| Factor I deficiency | 99 | CFI | |
| MAC inhibitor (CD59) deficiency | 103 | CD59 | |
| Mannose-binding lectin deficiency | |||
| Disease | Fact file | Gene | Animal models |
| Mannose-binding lectin deficiency | 96 | MBL2 | |
| Mannan-binding lectin - associated serine protease 2 deficiency | 119 | MASP2 | Mouse: |
| Periodic fever syndromes | |||
| Familial mediterranean fever | 140 | MEFV | Mouse: |
| Hyperimmunoglobulinemia D with periodic fever syndrome | 141 | MVK | Mouse: |
| Tumor necrosis factor receptor-associated periodic syndrome | 142 | TNFRSF1A | Mouse: Rat: |
| Cold autoinflammatory syndrome | |||
| Disease | Fact file | Gene | Animal models |
| Familial cold urticaria and Muckle-Wells syndrome | 143 | CIAS1 | Mouse: |
| Chronic infantile neurological cutaneous and articular syndrome | 144 | CIAS1 | Mouse: |
| Granulomatous sinovitis with uveitis and cranial neuropathies | 145 | CARD15 | Mouse: Rat: |
| Crohn's disease | 146 | CARD15 | Mouse: Rat: |