Incoming and outgoing links Primary immunodeficiencies and skin

Outgoing links

• ACP5 Gene
• ADA
• ADA2 Gene
• ADA Gene
• ADAM17gene
• ADAR Gene
• Agammaglobulinemia 3, mutation in CD79A
• Agammaglobulinemia C-chromosomal type bruton
• Agammaglobulinemia (Review)
• Aicardi-goutières syndrome
• Aire gene
• Angioedema hereditary
• Angioedema hereditary 1
• Ap1s3 gene
• Ataxia teleangiectatica
• Autoinflammatory Syndrome, Familial, Behcet-Like
• Bloom syndrome
• C1-esterase inhibitor
• C2 Gene
• C4A Gene
• Candle syndrome
• CARD11 Gene
• CARD14 Gene
• Cartilage-hair hypoplasia
• CD40LG Gene
• CD81 Gene
• CHARGE syndrome
• Chediak higashi syndrome
• Chilblain lupus
• Chronic granulomatous disease
• Chronic mucocutaneous candidiasis
• Comel-netherton syndrome
• Common variable immunodeficiency-13
• Complement Component 2 Deficiency
• Constitutional Mismatch Repair Deficiency Syndrom
• CVID
• CVID10
• CXCR4 Gene
• CYBB Gene
• DCLRE1C Gene
• DCTN1 Gene
• Digeorge syndrome
• DNASE1L3 Gene
• DNASE2 Gene
• DNMT3B Gene
• DOCK8
• DOCK8 Gene
• Dyschromatosis symmetrica hereditaria
• Dyskeratosis congenita
• Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency 2
• Ectodermale dysplasia, anhidrotic, with immundeficiency
• ELF4 Gene
• Familial cold autoinflammatory syndrome 3
• Familial cold autoinflammatory syndrome 4
• Familial cold-induced autoinflammatory syndrome 2
• Familial cold inflammatory syndrome 1
• Fanconi anaemia
• FCGR3A Gene
• FOXN1 Gene
• GATA2 Gene
• Hermansky-pudlak syndrome
• HIES
• Hyper-ige syndrome
• Hyper IgE syndrome 1
• Hyper IgE syndrome 3
• Hyper-IgE-syndrome 4, autosomal recessive
• Hyper-IgE-Syndrome 5
• Hyper IgM-Syndrome
• Hyperimmunoglobulin E syndrome type 2
• ICF syndrome
• IFNGR1 Gene
• IFNGR2 Gene
• IGAD1 Gene
• IgA vascultis (Henoch-Schoenlein purpura)
• IKZF1 Gene
• IL10 Gene
• IL12B Gene
• IL17F gene
• IL18BP Gene
• IL1RN
• IL2RA Gene
• IL2RG Gene
• IL6R Gene
• IL6ST gene
• Immundeficiency 14A (autosomal dominant), Mutation in PIK3CD
• Immundeficiency 20
• Interleukin-10
• Interleukin-18
• Interleukin-2
• IPEX
• IRAK1 Gene
• IRF8 Gene
• ITGB2 Gene
• Jacobsen syndrome
• JAK3-gene
• Keratosis palmoplantaris diffusa with mutations in cathepsin c
• LAD
• LIG1 Gene
• LIG4 syndrome
• Lipodystrophies
• Loeys-dietz syndrome
• MCM4 Gene
• MEFV Gene
• Mendelian susceptibility to mycobacterial diseases
• Muckle-wells syndrome
• MVK gene
• NCSTN Gene
• NEMO
• NFKB1 Gene
• NHEJ1 Gene
• Nijmegen breakage syndrome
• NLRC4 Gene
• NLRP12 Gene
• NLRP3 Gene
• Omenn syndrome
• OTULIN Gene
• Perry syndrome
• Pgm3 gene
• PID - Human Inborn Errors of Immunity
• PIK3CD Gene
• PIK3R1 Gene
• Pityriasis rubra pilaris (overview)
• PLCG2 Gene
• PMS2 Gene
• Poikiloderma with neutropenia
• POLA1 Gene
• Polyglandular autoimmune syndromes
• PSEN2 Gene
• PSMB8 Gene
• RAC2 Gene
• RAG1 gene
• Schimke Immunoosseous Dysplasia
• Selective deficiency of immunoglobulin A
• Severe combined Immunodefciency (overwiew)
• Severe T-Cell Immunodeficiency-Congenital Alopecia-Nail Dystrophy
• Shwachman-Bodian-Diamond syndrome
• SLC29A3 Gene
• SMARCAL1 Gene
• SPINK5 gene
• STAt1
• STAT1-gene
• STAT3-gene
• STAT5B-gene
• STING1-gene
• Subcutaneous panniculitis-like t-cell lymphoma
• Suppurative hidradenitis
• Sweet syndrome
• TAP1 Gene
• TAPBP Gene
• TIRAP Gene
• TNFAIP3 Gene
• TNFRSF13B gene
• Trex1 gene
• Trichorrhexis nodosa
• TTC37 Gene
• Urticaria vasculitis
• Verruciform epidermodysplasia
• Vici syndrome
• Whim syndrome
• Wiedemann-Steiner syndrome
• Wiskott-Aldrich syndrome
• Znf431 gene

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