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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Spinal epidural arteriovenous malformation

ORPHA:715326Morph.
Unknown

Spinal muscular atrophy with respiratory distress type 1

ORPHA:98920Disease
Autosomal recessive

Spinal muscular atrophy with respiratory distress type 2

ORPHA:404521Disease
Unknown

Spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome

ORPHA:73245Malform.
Unknown

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

ORPHA:2590Disease
Autosomal recessive

Spinal pial arteriovenous fistula

ORPHA:715302Disease
Not applicable

Spindle cell hemangioma

ORPHA:210584Disease
Not applicable

Spinocerebellar ataxia type 1

ORPHA:98755Disease
Autosomal dominant

Spinocerebellar ataxia type 10

ORPHA:98761Disease
Autosomal dominant

Spinocerebellar ataxia type 11

ORPHA:98767Disease
Autosomal dominant

Spinocerebellar ataxia type 12

ORPHA:98762Disease
Autosomal dominant

Spinocerebellar ataxia type 13

ORPHA:98768Disease
Autosomal dominant

Spinocerebellar ataxia type 14

ORPHA:98763Disease
Autosomal dominant

Spinocerebellar ataxia type 15/16

ORPHA:98769Disease
Autosomal dominant

Spinocerebellar ataxia type 17

ORPHA:98759Disease
Autosomal dominant

Spinocerebellar ataxia type 18

ORPHA:98771Disease
Autosomal dominant

Spinocerebellar ataxia type 19/22

ORPHA:98772Disease
Autosomal dominant

Spinocerebellar ataxia type 2

ORPHA:98756Disease
Autosomal dominant

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