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Hyperimmunoglobulinemia D with periodic fever

ORPHA:343Clinical subtypeAutosomal recessiveInfancy

Ассоциированные гены (1)

MVK
mevalonate kinase
Disease-causing germline mutation(s) in
OMIM: 251170

Фенотипы (26)

Очень частый (80–99%)9
HP:0001954Recurrent fever
HP:0002027Abdominal pain
HP:0002239Gastrointestinal hemorrhage
HP:0002240Hepatomegaly
HP:0002716Lymphadenopathy
HP:0002829Arthralgia
HP:0003261Increased circulating IgA level
HP:0003326Myalgia
HP:0003565Elevated erythrocyte sedimentation rate
Частый (30–79%)7
HP:0001025Urticaria
HP:0001369Arthritis
HP:0002014Diarrhea
HP:0002076Migraine
HP:0002633Vasculitis
HP:0011107Recurrent aphthous stomatitis
HP:0200034Papule
Периодический (5–29%)10
HP:0000979Purpura
HP:0001063Acrocyanosis
HP:0001250Seizure
HP:0001251Ataxia
HP:0001263Global developmental delay
HP:0001376Limitation of joint mobility
HP:0001510Growth delay
HP:0002586Peritonitis
HP:0005214Intestinal obstruction
HP:0010783Erythema

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы