Molekulargenetisches Labor
Zentrum für Nephrologie und Stoffwechsel
Moldiag Erkrankungen Gene Support Kontakt

Hereditäre maligne Bluterkrankungen

Unter hereditären malignen Bluerkrankungen werden genetische Störungen zusammengefasst die mit einer höheren Wahrscheinlichkeit von Blutkrebserkrankungen einhergehen.

Gliederung

Erbliche Blutkrankheiten und Gerinnungsstörungen
Aplastische Anämie
Autoimmun-lymphoproliferatives Syndrom 5
Erbliche Blutungsübel
Familiäre Erythrozytose 2
Familiäre hämophygozytische Lymphohistiozytose
H-Syndrom
Hereditäre Thrombozytenerkrankungen
Hereditäre maligne Bluterkrankungen
Akute myeloische Leukämie
JAK2
Erbliche Anfälligkeit für akute myeloische Leukämie
GATA2
Erbliche Anfälligkeit für myelodysplastisches Syndrom
GATA2
Juvenile myelomonozyäre Leukämie
NF1
Lymphoproliferatives Syndrom
Autoimmun-lymphoproliferatives Syndrom Typ 2
CASP10
Lymphoproliferatives Syndrom 1
ITK
X-chromosomales lymphoproliferatives Syndrom 1
SH2D1A
X-chromosomales lymphoproliferatives Syndrom 2
XIAP
Myelodysplastisches Syndrom
ASXL1
Non-Hodgkin-Lymphom
CASP10
Noonan-Syndrom ähnliches Krankheitsbild und juvenile myelomonozytische Leukämie
CBL
Osteomyelofibrose
JAK2
Polycythaemia vera
JAK2
Somatische Erythrozytose
JAK2
Kongenitale sideroblastische Anämie-B-Zell-Immundefekt-periodisches Fieber-Entwicklungsverzögerungs-Syndrom
MIRAGE-Syndrom
Ovalozytose
Paroxysmale nächtliche Hämoglobinurie
Retinitis pigmentosa mit Mikrozytose
Störungen des Cobalaminstoffwechsels
Vaskulitis durch ADA2-Mangel
Venöse thromboembolische Erkrankungen

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Gelsi-Boyer V et al. (2009) Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.

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Update: 14. August 2020
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