Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Spinal epidural arteriovenous malformation
Unknown
Spinal muscular atrophy with respiratory distress type 1
Autosomal recessive
Infancy, Neonatal
Spinal muscular atrophy with respiratory distress type 2
Unknown
Neonatal
Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome
Unknown
Infancy, Neonatal
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome
Autosomal recessive
Childhood
Spinal pial arteriovenous fistula
Not applicable
Spindle cell hemangioma
Not applicable
Adolescent, Adult, Childhood, Elderly
Spinocerebellar ataxia type 1
Autosomal dominant
All ages
Spinocerebellar ataxia type 10
Autosomal dominant
Adult
Spinocerebellar ataxia type 11
Autosomal dominant
Adolescent, Adult, Childhood, Elderly
Spinocerebellar ataxia type 12
Autosomal dominant
All ages
Spinocerebellar ataxia type 13
Autosomal dominant
Adult
Spinocerebellar ataxia type 14
Autosomal dominant
Adolescent, Adult, Childhood, Elderly
Spinocerebellar ataxia type 15/16
Autosomal dominant
Adult, Elderly
Spinocerebellar ataxia type 17
Autosomal dominant
All ages
Spinocerebellar ataxia type 18
Autosomal dominant
Adult
Spinocerebellar ataxia type 19/22
Autosomal dominant
Adult
Spinocerebellar ataxia type 2
Autosomal dominant
All ages
Spinocerebellar ataxia type 20
Autosomal dominant
Adult
Spinocerebellar ataxia type 21
Autosomal dominant
Adolescent
Spinocerebellar ataxia type 23
Autosomal dominant
Adult
Spinocerebellar ataxia type 25
Autosomal dominant
All ages
Spinocerebellar ataxia type 26
Autosomal dominant
Adult
Spinocerebellar ataxia type 27A
Autosomal dominant
Adolescent, Adult