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GJC2-related late-onset primary lymphedema

ORPHA:568051DiseaseAutosomal dominantAdolescent, Adult, Childhood

Ассоциированные гены (1)

GJC2
gap junction protein gamma 2
Disease-causing germline mutation(s) in
OMIM: 608803

Фенотипы (13)

Частый (30–79%)5
HP:0001785Ankle swelling
HP:0003550Predominantly lower limb lymphedema
HP:0003759Hypoplasia of lymphatic vessels
HP:0010741Pedal edema
HP:0100766Abnormal lymphatic vessel morphology
Периодический (5–29%)6
HP:0000282Facial edema
HP:0001581Recurrent skin infections
HP:0002619Varicose veins
HP:0005293Venous insufficiency
HP:0007514Edema of the dorsum of hands
HP:0100658Cellulitis
Очень редкий (1–4%)2
HP:0000508Ptosis
HP:0031188Genital edema

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы