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Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency

ORPHA:319552DiseaseAutosomal recessiveChildhood

Ассоциированные гены (1)

IL12RB1
interleukin 12 receptor subunit beta 1
Disease-causing germline mutation(s) in
OMIM: 601604

Фенотипы (15)

Очень частый (80–99%)4
HP:0011117Abnormal circulating interleukin concentration
HP:0011274Recurrent mycobacterial infections
HP:0002721Immunodeficiency
HP:0020087BCGosis
Частый (30–79%)3
HP:0032283Disseminated nontuberculous mycobacterial infection
HP:0005401Recurrent candida infections
HP:0002840Lymphadenitis
Периодический (5–29%)3
HP:0005661Salmonella osteomyelitis
HP:0007408Tegumentary leishmaniasis susceptibility
HP:0002090Pneumonia
Очень редкий (1–4%)5
HP:0200029Vasculitis in the skin
HP:0002742Recurrent Klebsiella infections
HP:0032256Histoplasmosis
HP:0032249Coccidioidomycosis
HP:0020105Severe toxoplasmosis

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