Seltene Erkrankungen (Orphan)
Komplette Bibliothek mit 7,547 Erkrankungen — Genetik, Phänotypen, Epidemiologie, Orphan-Arzneimittel und Studien.
Spinocerebellar ataxia type 27B
Autosomal dominant
Spinocerebellar ataxia type 28
Autosomal dominant
Childhood
Spinocerebellar ataxia type 29
Autosomal dominant, Autosomal recessive
Infancy, Neonatal
Spinocerebellar ataxia type 3
Autosomal dominant
Adult, Childhood
Spinocerebellar ataxia type 30
Autosomal dominant
Adult, Elderly
Spinocerebellar ataxia type 31
Autosomal dominant
Adolescent, Adult, Childhood, Elderly
Spinocerebellar ataxia type 32
Autosomal dominant
Adult
Spinocerebellar ataxia type 34
Autosomal dominant
Adolescent, Adult, Neonatal
Spinocerebellar ataxia type 35
Autosomal dominant
Adolescent, Adult
Spinocerebellar ataxia type 36
Autosomal dominant
Adult
Spinocerebellar ataxia type 37
Autosomal dominant
Adult
Spinocerebellar ataxia type 38
Autosomal dominant
Adult
Spinocerebellar ataxia type 4
Autosomal dominant
Adult
Spinocerebellar ataxia type 40
Autosomal dominant
Adult
Spinocerebellar ataxia type 41
Autosomal dominant
Adult
Spinocerebellar ataxia type 42
Autosomal dominant
Adolescent, Adult, Childhood, Elderly
Spinocerebellar ataxia type 43
Autosomal dominant
Adult, Elderly
Spinocerebellar ataxia type 44
Autosomal dominant
Adult
Spinocerebellar ataxia type 45
Autosomal dominant
Adult
Spinocerebellar ataxia type 46
Autosomal dominant
Adult
Spinocerebellar ataxia type 48
Autosomal dominant
Adult
Spinocerebellar ataxia type 49
Autosomal dominant
Adolescent, Adult, Childhood
Spinocerebellar ataxia type 5
Autosomal dominant
Adolescent, Adult, Childhood, Elderly
Spinocerebellar ataxia type 6
Autosomal dominant
Adolescent, Adult, Elderly