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Microcephalic osteodysplastic dysplasia, Saul-Wilson type

ORPHA:85172DiseaseAutosomal recessiveNeonatal

Ассоциированные гены (1)

COG4
component of oligomeric golgi complex 4
Disease-causing germline mutation(s) in
OMIM: 606976

Фенотипы (16)

Очень частый (80–99%)16
HP:0000252Microcephaly
HP:0000272Malar flattening
HP:0000444Convex nasal ridge
HP:0000446Narrow nasal bridge
HP:0000518Cataract
HP:0000520Proptosis
HP:0000926Platyspondyly
HP:0001762Talipes equinovarus
HP:0002007Frontal bossing
HP:0003311Hypoplasia of the odontoid process
HP:0004279Short palm
HP:0004322Short stature
HP:0004582Irregularity of vertebral bodies
HP:0010230Cone-shaped epiphyses of the phalanges of the hand
HP:0011833Overhanging nasal tip
HP:0200055Small hand

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