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Combined immunodeficiency due to DOCK8 deficiency

ORPHA:217390DiseaseAutosomal recessiveInfancy, Neonatal

Ассоциированные гены (1)

DOCK8
dedicator of cytokinesis 8
Disease-causing germline mutation(s) in
OMIM: 611432

Фенотипы (18)

Очень частый (80–99%)15
HP:0000389Chronic otitis media
HP:0001047Atopic dermatitis
HP:0002090Pneumonia
HP:0002099Asthma
HP:0002205Recurrent respiratory infections
HP:0003212Increased circulating IgE level
HP:0004429Recurrent viral infections
HP:0005401Recurrent candida infections
HP:0005403Decreased total T cell count
HP:0005406Recurrent bacterial skin infections
HP:0010976Decreased total B cell count
HP:0011108Recurrent sinusitis
HP:0012203Onychomycosis
HP:0200042Skin ulcer
HP:0200043Verrucae
Периодический (5–29%)3
HP:0002860Squamous cell carcinoma
HP:0006763Anal canal squamous carcinoma
HP:0030417Squamous cell carcinoma of the vulva

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы