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Incoming and outgoing links Immundefekte primäre (kombinierte ID mit assoziierten oder syndromalen Eigenschaften)

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Incoming links

  • Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature
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Outgoing links

  • AIDS Related Complex
  • Albinismus (Übersicht)
  • Anhidrotische ektodermale Dysplasie
  • ARPC1B-Gen
  • Ataxia teleangiectatica (Louis-Bar-Syndrom)
  • ATM-Gen
  • Bloom-Syndrom
  • CARD11-Gen
  • Knorpel-Haar-Hypoplasie
  • CCBE1-Gen
  • CDG-Syndrome
  • Comel-Netherton-Syndrom
  • DiGeorge-Syndrom
  • DOCK8-Gen
  • Anhidrotische ektodermale Dysplasie mit Immundefizienz 2
  • Anhidrotische ektodermale Dysplasie mit Immundefizienz 1
  • Eosinophilie
  • EPG5-Gen
  • ERBIN-Gen
  • FOXN1-Gen
  • Hennekam-Lymphangiektasie-Lymphödem Syndrom Typ1
  • Hyper-IgE-Syndrom (Übersicht)
  • Hyper-IgE-Syndrom 1
  • Hyper-IgE-Syndrom 3
  • Hyper-IgE-Syndrom 4
  • Hyper-IgE-Syndrom 5
  • Hyper-IgE-Syndrom 2
  • IgA-Nephropathie
  • IgE
  • IKBKB-Gen
  • IKBKG-Gen
  • IL6R-Gen
  • IL6ST-Gen
  • Immundefizienz 7
  • Immundefizienz 9
  • Immundefizienz 96 und LIG1-Defekt
  • Interleukin-15
  • Jacobsen-Syndrom
  • KMT2A-Gen
  • LEKTI
  • LIG1-Gen
  • Loeys-Dietz-Syndrom
  • MCM4-Gen
  • Mikrodeletions-Syndrom 22q11
  • NF-kappaB
  • NFKBIA-Gen
  • Nijmegen-Breakage-Syndrom
  • NSMCE3-Gen
  • ORAI1-Gen
  • PGM3-Gen
  • Schimke-Immunoossäre Dysplasie
  • SEMA3E-Gen
  • SCID (Übersicht)
  • SPINK5-Gen
  • STAT3-Gen
  • STAT5B-Gen
  • STIM1-Gen
  • T-Zelle regulatorische
  • TGFBR1-Gen
  • Th17-Zelle
  • Trichohepatoenterisches Syndrom 1
  • TTC37-Gen
  • Vici-Syndrom
  • WAS-Gen
  • Wiedemann-Steiner-Syndrom
  • WIPF1-Gen
  • Wiskott-Aldrich-Syndrom
  • Wiskott-Aldrich-Syndrom-2
  • Kräuselhaar angeborenes
  • ZNF431-Gen
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