← Назад

Multiple epiphyseal dysplasia type 1

ORPHA:93308DiseaseAutosomal dominantChildhood

Ассоциированные гены (1)

COMP
cartilage oligomeric matrix protein
Disease-causing germline mutation(s) in
OMIM: 600310

Фенотипы (21)

Частый (30–79%)6
HP:0001288Gait disturbance
HP:0001385Hip dysplasia
HP:0003026Short long bone
HP:0003365Arthralgia of the hip
HP:0030839Knee pain
HP:0030973Postexertional malaise
Периодический (5–29%)10
HP:0001376Limitation of joint mobility
HP:0001387Joint stiffness
HP:0002515Waddling gait
HP:0002663Delayed epiphyseal ossification
HP:0002758Osteoarthritis
HP:0003170Abnormality of the acetabulum
HP:0003498Disproportionate short stature
HP:0006094Finger joint hypermobility
HP:0030840Ankle pain
HP:0045086Knee joint hypermobility
Очень редкий (1–4%)4
HP:0002812Coxa vara
HP:0002857Genu valgum
HP:0002970Genu varum
HP:0005743Avascular necrosis of the capital femoral epiphysis
Исключён (0%)1
HP:0001156Brachydactyly

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы