Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Autosomal dominant spastic paraplegia type 10
Autosomal dominant
Adolescent, Adult, Childhood
Autosomal dominant spastic paraplegia type 12
Autosomal dominant
Adolescent, Adult, Childhood
Autosomal dominant spastic paraplegia type 13
Autosomal dominant
Adolescent, Adult
Autosomal dominant spastic paraplegia type 17
Autosomal dominant
Adolescent, Adult, Childhood
Autosomal dominant spastic paraplegia type 19
Autosomal dominant
Adult
Autosomal dominant spastic paraplegia type 29
Autosomal dominant
Adolescent
Autosomal dominant spastic paraplegia type 3
Autosomal dominant
Adult, Childhood
Autosomal dominant spastic paraplegia type 31
Autosomal dominant
Childhood
Autosomal dominant spastic paraplegia type 36
Autosomal dominant
Adolescent, Adult
Autosomal dominant spastic paraplegia type 37
Autosomal dominant
All ages
Autosomal dominant spastic paraplegia type 38
Autosomal dominant
Childhood
Autosomal dominant spastic paraplegia type 4
Autosomal dominant
Adolescent, Adult, Childhood, Infancy
Autosomal dominant spastic paraplegia type 41
Autosomal dominant
Adolescent, Adult
Autosomal dominant spastic paraplegia type 42
Autosomal dominant
Adolescent, Adult, Childhood
Autosomal dominant spastic paraplegia type 6
Autosomal dominant
Adolescent, Adult, Childhood
Autosomal dominant spastic paraplegia type 73
Autosomal dominant
Adult
Autosomal dominant spastic paraplegia type 8
Autosomal dominant
Adolescent, Adult
Autosomal dominant spastic paraplegia type 80
Autosomal dominant
Adolescent, Childhood
Autosomal dominant spastic paraplegia type 9A
Autosomal dominant
Adolescent, Adult, Infancy
Autosomal dominant spastic paraplegia type 9B
Autosomal dominant
Adolescent, Adult, Infancy
Autosomal dominant spondylocostal dysostosis
Autosomal dominant
No data available
Autosomal dominant striatal neurodegeneration
Autosomal dominant
Adult
Autosomal dominant thrombocytopenia with platelet secretion defect
Autosomal dominant
Childhood
Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant
Adolescent, Adult, Childhood, Infancy