Orphanet Datenbank · Orphadata CC-BY-4.0

Seltene Erkrankungen (Orphan)

Komplette Bibliothek mit 7,547 Erkrankungen — Genetik, Phänotypen, Epidemiologie, Orphan-Arzneimittel und Studien.

7,547

Erkrankungen

4 552

Gene

8 700

Phänotypen

140

Regionen

Diagnose-Assistent Arzneimittelsuche Klinische Studien Statistik

Alle (7,547)Bio-Anomalie Kategorie Klinische Gruppe Klinischer Subtyp Clinical syndrome Erkrankung Ätiologischer Subtyp Histopathologischer Subtyp Malformationssyndrom Morphologische Anomalie Besondere klinische Situation

3,968 Erkrankungen gefunden (Typ: Erkrankung)

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Autosomal recessive spastic paraplegia type 66

ORPHA:401815Erkrankung

Autosomal recessive

Infancy

Autosomal recessive spastic paraplegia type 67

ORPHA:401820Erkrankung

Autosomal recessive

Childhood, Infancy

Autosomal recessive spastic paraplegia type 69

ORPHA:401830Erkrankung

Autosomal recessive

Infancy

Autosomal recessive spastic paraplegia type 70

ORPHA:401835Erkrankung

Autosomal recessive

Infancy

Autosomal recessive spastic paraplegia type 71

ORPHA:401840Erkrankung

Autosomal recessive

Infancy

Autosomal recessive spastic paraplegia type 74

ORPHA:468661Erkrankung

Autosomal recessive

Childhood

Autosomal recessive spastic paraplegia type 75

ORPHA:459056Erkrankung

Autosomal recessive

Childhood

Autosomal recessive spastic paraplegia type 76

ORPHA:488594Erkrankung

Autosomal recessive

Adult

Autosomal recessive spastic paraplegia type 77

ORPHA:466722Erkrankung

Autosomal recessive

Childhood, Infancy

Autosomal recessive spastic paraplegia type 78

ORPHA:513436Erkrankung

Autosomal recessive

Adolescent, Adult, Childhood

Autosomal recessive spastic paraplegia type 82

ORPHA:631073Erkrankung

Autosomal recessive

Childhood, Infancy

Autosomal recessive spastic paraplegia type 83

ORPHA:631076Erkrankung

Autosomal recessive

Adolescent, Childhood

Autosomal recessive spastic paraplegia type 84

ORPHA:631079Erkrankung

Autosomal recessive

Childhood, Infancy

Autosomal recessive spastic paraplegia type 85

ORPHA:631082Erkrankung

Autosomal recessive

Childhood, Infancy

Autosomal recessive spastic paraplegia type 86

ORPHA:631085Erkrankung

Autosomal recessive

Childhood, Infancy

Autosomal recessive spastic paraplegia type 87

ORPHA:631088Erkrankung

Autosomal recessive

Childhood, Infancy

Autosomal recessive spastic paraplegia type 9B

ORPHA:447760Erkrankung

Autosomal recessive

Childhood, Infancy

Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome

ORPHA:95433Erkrankung

Autosomal recessive

Childhood

Autosomal semi-dominant severe lipodystrophic laminopathy

ORPHA:280365Erkrankung

Semi-dominant

Adult