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Phosphoribosylpyrophosphate synthetase superactivity

ORPHA:3222DiseaseX-linked recessiveAdolescent, Adult, Childhood, Infancy, Neonatal

Фенотипы (13)

Очень частый (80–99%)3
HP:0000407Sensorineural hearing impairment
HP:0001251Ataxia
HP:0002149Hyperuricemia
Частый (30–79%)5
HP:0000083Renal insufficiency
HP:0001249Intellectual disability
HP:0001252Hypotonia
HP:0001679Abnormal aortic morphology
HP:0002167Abnormality of speech or vocalization
Периодический (5–29%)5
HP:0000486Strabismus
HP:0000496Abnormality of eye movement
HP:0000822Hypertension
HP:0001638Cardiomyopathy
HP:0011675Arrhythmia

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