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Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency

ORPHA:329249Etiological subtypeAutosomal dominantChildhood

Ассоциированные гены (1)

SH2B1
SH2B adaptor protein 1
Disease-causing germline mutation(s) (loss of function) in
OMIM: 608937

Фенотипы (11)

Очень частый (80–99%)5
HP:0000842Hyperinsulinemia
HP:0001513Obesity
HP:0002591Polyphagia
HP:0004322Short stature
HP:0012760Reduced social responsiveness
Частый (30–79%)3
HP:0000718Aggressive behavior
HP:0000750Delayed speech and language development
HP:0008763No social interaction
Исключён (0%)3
HP:0002910Elevated circulating hepatic transaminase concentration
HP:0003074Hyperglycemia
HP:0003077Hyperlipidemia

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