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

Familiäre hämophygozytische Lymphohistiozytose

Familiäre hämophygozytische Lymphohistiozytose ist eine genetische Erkrankung, deren Locus noch nicht bei allen Untergruppen definiert werden konnte. Die Erkrankung ist durch eine Panzytopenie gekennzeichnet, die sowohl auf eine Phagozytose der Blutzellen wie auch auf eine Histiozytose des Knochenmaks zurückzuführen ist.

Gliederung

Erbliche Blutkrankheiten und Gerinnungsstörungen
Aplastische Anämie
Autoimmun-lymphoproliferatives Syndrom 5
Erbliche Blutungsübel
Familiäre Erythrozytose 2
Familiäre hämophygozytische Lymphohistiozytose
Familiäre hämophygozytische Lymphohistiozytose 1
Familiäre hämophygozytische Lymphohistiozytose 2
PRF1
Familiäre hämophygozytische Lymphohistiozytose 3
UNC13D
Familiäre hämophygozytische Lymphohistiozytose 4
STX11
Familiäre hämophygozytische Lymphohistiozytose 5
STXBP2
H-Syndrom
Hereditäre Thrombozytenerkrankungen
Hereditäre maligne Bluterkrankungen
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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Update: 14. August 2020
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