MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Spinal epidural arteriovenous malformation

ORPHA:715326Morph.
Unknown

Spinal muscular atrophy with respiratory distress type 1

ORPHA:98920Kr.
Autosomal recessive

Spinal muscular atrophy with respiratory distress type 2

ORPHA:404521Kr.
Unknown

Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome

ORPHA:73245Malf.
Unknown

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

ORPHA:2590Kr.
Autosomal recessive

Spinal pial arteriovenous fistula

ORPHA:715302Kr.
Not applicable

Spindle cell hemangioma

ORPHA:210584Kr.
Not applicable

Spinocerebellar ataxia type 1

ORPHA:98755Kr.
Autosomal dominant

Spinocerebellar ataxia type 10

ORPHA:98761Kr.
Autosomal dominant

Spinocerebellar ataxia type 11

ORPHA:98767Kr.
Autosomal dominant

Spinocerebellar ataxia type 12

ORPHA:98762Kr.
Autosomal dominant

Spinocerebellar ataxia type 13

ORPHA:98768Kr.
Autosomal dominant

Spinocerebellar ataxia type 14

ORPHA:98763Kr.
Autosomal dominant

Spinocerebellar ataxia type 15/16

ORPHA:98769Kr.
Autosomal dominant

Spinocerebellar ataxia type 17

ORPHA:98759Kr.
Autosomal dominant

Spinocerebellar ataxia type 18

ORPHA:98771Kr.
Autosomal dominant

Spinocerebellar ataxia type 19/22

ORPHA:98772Kr.
Autosomal dominant

Spinocerebellar ataxia type 2

ORPHA:98756Kr.
Autosomal dominant

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