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Opsismodysplasia

ORPHA:2746DiseaseAutosomal recessiveNeonatal

Ассоциированные гены (1)

INPPL1
inositol polyphosphate phosphatase like 1
Disease-causing germline mutation(s) in
OMIM: 600829

Фенотипы (27)

Очень частый (80–99%)17
HP:0000239Large fontanelles
HP:0000256Macrocephaly
HP:0000944Abnormal metaphysis morphology
HP:0001156Brachydactyly
HP:0001182Tapered finger
HP:0002007Frontal bossing
HP:0002093Respiratory insufficiency
HP:0002750Delayed skeletal maturation
HP:0003173Hypoplastic pubic bone
HP:0003175Hypoplastic ischia
HP:0003177Squared iliac bones
HP:0003196Short nose
HP:0003510Severe short stature
HP:0005280Depressed nasal bridge
HP:0005930Abnormality of epiphysis morphology
HP:0008479Hypoplastic vertebral bodies
HP:0100569Abnormally ossified vertebrae
Частый (30–79%)3
HP:0001252Hypotonia
HP:0002205Recurrent respiratory infections
HP:0005469Flat occiput
Периодический (5–29%)7
HP:0000592Blue sclerae
HP:0000767Pectus excavatum
HP:0000774Narrow chest
HP:0001387Joint stiffness
HP:0001744Splenomegaly
HP:0002240Hepatomegaly
HP:0011304Broad thumb

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