← Назад

Waldenström macroglobulinemia

ORPHA:33226DiseaseMultigenic/multifactorialElderly

Ассоциированные гены (1)

MYD88
MYD88 innate immune signal transduction adaptor
Disease-causing somatic mutation(s) in
OMIM: 602170

Фенотипы (45)

Очень частый (80–99%)3
HP:0001909Leukemia
HP:0002665Lymphoma
HP:0005508Monoclonal immunoglobulin M proteinemia
Частый (30–79%)7
HP:0000225Gingival bleeding
HP:0000980Pallor
HP:0001874Abnormality of neutrophils
HP:0001897Normocytic anemia
HP:0002093Respiratory insufficiency
HP:0002321Vertigo
HP:0100724Hypercoagulability
Периодический (5–29%)35
HP:0000083Renal insufficiency
HP:0000365Hearing impairment
HP:0000421Epistaxis
HP:0000520Proptosis
HP:0000573Retinal hemorrhage
HP:0000965Cutis marmorata
HP:0000979Purpura
HP:0001025Urticaria
HP:0001251Ataxia
HP:0001297Stroke
HP:0001635Congestive heart failure
HP:0001744Splenomegaly
HP:0001945Fever
HP:0002014Diarrhea
HP:0002024Malabsorption
HP:0002039Anorexia
HP:0002076Migraine
HP:0002113Pulmonary infiltrates
HP:0002202Pleural effusion
HP:0002239Gastrointestinal hemorrhage
HP:0002240Hepatomegaly
HP:0002354Memory impairment
HP:0002633Vasculitis
HP:0002716Lymphadenopathy
HP:0002719Recurrent infections
HP:0003565Elevated erythrocyte sedimentation rate
HP:0004372Reduced consciousness/confusion
HP:0006824Cranial nerve paralysis
HP:0008046Abnormal retinal vascular morphology
HP:0009830Peripheral neuropathy
HP:0010741Pedal edema
HP:0010841Multifocal epileptiform discharges
HP:0012378Fatigue
HP:0100539Periorbital edema
HP:0100778Cryoglobulinemia

Эпидемиология (7)

Annual incidence
1-9 / 1 000 000
Europe
Annual incidence
1-9 / 100 000
France
Annual incidence
1-9 / 1 000 000
United States
Annual incidence
1-9 / 1 000 000
United Kingdom
Annual incidence
1-9 / 1 000 000
Spain
Point prevalence
Unknown
Worldwide
Point prevalence
1-9 / 100 000
Europe

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы