MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Spinocerebellar ataxia type 20

ORPHA:101110Disease
Autosomal dominant

Spinocerebellar ataxia type 21

ORPHA:98773Disease
Autosomal dominant

Spinocerebellar ataxia type 23

ORPHA:101108Disease
Autosomal dominant

Spinocerebellar ataxia type 25

ORPHA:101111Disease
Autosomal dominant

Spinocerebellar ataxia type 26

ORPHA:101112Disease
Autosomal dominant

Spinocerebellar ataxia type 27A

ORPHA:98764Disease
Autosomal dominant

Spinocerebellar ataxia type 27B

ORPHA:675216Disease
Autosomal dominant

Spinocerebellar ataxia type 28

ORPHA:101109Disease
Autosomal dominant

Spinocerebellar ataxia type 29

ORPHA:208513Disease
Autosomal dominant, Autosomal recessive

Spinocerebellar ataxia type 3

ORPHA:98757Disease
Autosomal dominant

Spinocerebellar ataxia type 30

ORPHA:211017Disease
Autosomal dominant

Spinocerebellar ataxia type 31

ORPHA:217012Disease
Autosomal dominant

Spinocerebellar ataxia type 32

ORPHA:276183Disease
Autosomal dominant

Spinocerebellar ataxia type 34

ORPHA:1955Disease
Autosomal dominant

Spinocerebellar ataxia type 35

ORPHA:276193Disease
Autosomal dominant

Spinocerebellar ataxia type 36

ORPHA:276198Disease
Autosomal dominant

Spinocerebellar ataxia type 37

ORPHA:363710Disease
Autosomal dominant

Spinocerebellar ataxia type 38

ORPHA:423296Disease
Autosomal dominant

Spinocerebellar ataxia type 4

ORPHA:98765Disease
Autosomal dominant

Spinocerebellar ataxia type 40

ORPHA:423275Disease
Autosomal dominant

Spinocerebellar ataxia type 41

ORPHA:458798Disease
Autosomal dominant

Spinocerebellar ataxia type 42

ORPHA:458803Disease
Autosomal dominant

Spinocerebellar ataxia type 43

ORPHA:497764Disease
Autosomal dominant

Spinocerebellar ataxia type 44

ORPHA:631095Disease
Autosomal dominant