MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Spinocerebellar ataxia type 20

ORPHA:101110Kr.
Autosomal dominant

Spinocerebellar ataxia type 21

ORPHA:98773Kr.
Autosomal dominant

Spinocerebellar ataxia type 23

ORPHA:101108Kr.
Autosomal dominant

Spinocerebellar ataxia type 25

ORPHA:101111Kr.
Autosomal dominant

Spinocerebellar ataxia type 26

ORPHA:101112Kr.
Autosomal dominant

Spinocerebellar ataxia type 27A

ORPHA:98764Kr.
Autosomal dominant

Spinocerebellar ataxia type 27B

ORPHA:675216Kr.
Autosomal dominant

Spinocerebellar ataxia type 28

ORPHA:101109Kr.
Autosomal dominant

Spinocerebellar ataxia type 29

ORPHA:208513Kr.
Autosomal dominant, Autosomal recessive

Spinocerebellar ataxia type 3

ORPHA:98757Kr.
Autosomal dominant

Spinocerebellar ataxia type 30

ORPHA:211017Kr.
Autosomal dominant

Spinocerebellar ataxia type 31

ORPHA:217012Kr.
Autosomal dominant

Spinocerebellar ataxia type 32

ORPHA:276183Kr.
Autosomal dominant

Spinocerebellar ataxia type 34

ORPHA:1955Kr.
Autosomal dominant

Spinocerebellar ataxia type 35

ORPHA:276193Kr.
Autosomal dominant

Spinocerebellar ataxia type 36

ORPHA:276198Kr.
Autosomal dominant

Spinocerebellar ataxia type 37

ORPHA:363710Kr.
Autosomal dominant

Spinocerebellar ataxia type 38

ORPHA:423296Kr.
Autosomal dominant

Spinocerebellar ataxia type 4

ORPHA:98765Kr.
Autosomal dominant

Spinocerebellar ataxia type 40

ORPHA:423275Kr.
Autosomal dominant

Spinocerebellar ataxia type 41

ORPHA:458798Kr.
Autosomal dominant

Spinocerebellar ataxia type 42

ORPHA:458803Kr.
Autosomal dominant

Spinocerebellar ataxia type 43

ORPHA:497764Kr.
Autosomal dominant

Spinocerebellar ataxia type 44

ORPHA:631095Kr.
Autosomal dominant