Verweise von und zu PID - deficiency of complement
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- 3MC Syndrome
- Aids
- Anaphylatoxins
- Angioedema (overview)
- AP50
- Apoptosis
- C1QA Gene
- C1QB Gene
- C1QC Gene
- C1q deficiency
- C1S Gene
- Complement Component 2 Deficiency
- C2 Gene
- Complement component 3 deficiency, autosomal recessive
- C3 Gene
- C4a-Defizienz-Syndrom, autosomal rezessives
- C4A Gene
- Complement component 5 deficiency
- C5 Gene
- C6 deficiency, subtotal included
- C6 Gene
- C8A Gene
- C8B Gene
- Complement Component 8 Deficiency, Type 1
- C8G Gene
- C9 Gene
- Cd46
- Cd55
- Cd59
- CFB Gene
- CFD Gene
- CFH Gene
- CFI Gene
- CFP Gene
- CH50
- COLEC11 Gene
- Dermatomyositis (overview)
- Leiner's disease
- Factor H-related proteins
- FCN3 Gene
- Primary ficolin-3 deficiency
- Hemolytic uremic syndrome
- Immunodeficiency Due to a Late Component of Complement Deficiency
- Complement factor H deficiency
- Complement factor I deficiency
- Complement system
- Lupus erythematosus systemic
- Masp2 Deficiency
- MASP2 Gene
- Membrane attack complex
- Membranoproliferative glomerulonephritis
- Neisseria meningitidis
- Periodontal ehlers-danlos syndrome
- Primary immunodeficiency
- Properdin
- Properdin-Deficiency, X-chromosomal
- Serine protease
- SERPING1 Gene
- THBD Gene
- Thrombin
- Thrombomodulin