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Hypophosphatasia

ORPHA:436DiseaseAutosomal dominant, Autosomal recessiveAll ages

Фенотипы (20)

Очень частый (80–99%)13
HP:0000164Abnormality of the dentition
HP:0000239Large fontanelles
HP:0000772Abnormal rib morphology
HP:0000774Narrow chest
HP:0000944Abnormal metaphysis morphology
HP:0001024Skin dimple over apex of long bone angulation
HP:0001363Craniosynostosis
HP:0001531Failure to thrive in infancy
HP:0002097Emphysema
HP:0004322Short stature
HP:0006487Bowing of the long bones
HP:0008872Feeding difficulties in infancy
HP:0010781Skin dimple
Частый (30–79%)7
HP:0000737Irritability
HP:0001250Seizure
HP:0001252Hypotonia
HP:0001903Anemia
HP:0002093Respiratory insufficiency
HP:0002757Recurrent fractures
HP:0003072Hypercalcemia

Эпидемиология (2)

Point prevalence
Unknown
Worldwide
Point prevalence
<1 / 1 000 000
China

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы