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Otoonychoperoneal syndrome

ORPHA:2793Malformation syndromeAutosomal recessiveAntenatal, Neonatal

Фенотипы (13)

Очень частый (80–99%)11
HP:0000400Macrotia
HP:0000940Abnormal diaphysis morphology
HP:0001256Intellectual disability, mild
HP:0001371Flexion contracture
HP:0001597Abnormality of the nail
HP:0006380Knee flexion contracture
HP:0008577Underfolded helix
HP:0009738Abnormality of the antihelix
HP:0009756Popliteal pterygium
HP:0009906Aplasia/Hypoplasia of the earlobes
HP:0011039Abnormality of the helix
Частый (30–79%)2
HP:0000268Dolichocephaly
HP:0000582Upslanted palpebral fissure

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