MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Autosomal dominant spastic paraplegia type 10

ORPHA:100991Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 12

ORPHA:100993Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 13

ORPHA:100994Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 17

ORPHA:100998Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 19

ORPHA:100999Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 29

ORPHA:101009Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 3

ORPHA:100984Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 31

ORPHA:101011Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 36

ORPHA:320365Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 37

ORPHA:171612Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 38

ORPHA:171617Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 4

ORPHA:100985Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 41

ORPHA:320355Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 42

ORPHA:171863Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 6

ORPHA:100988Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 73

ORPHA:444099Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 8

ORPHA:100989Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 80

ORPHA:631068Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 9A

ORPHA:447753Kr.
Autosomal dominant

Autosomal dominant spastic paraplegia type 9B

ORPHA:447757Kr.
Autosomal dominant

Autosomal dominant spondylocostal dysostosis

ORPHA:1797Malf.
Autosomal dominant

Autosomal dominant striatal neurodegeneration

ORPHA:228169Kr.
Autosomal dominant

Autosomal dominant thrombocytopenia with platelet secretion defect

ORPHA:466806Kr.
Autosomal dominant

Autosomal dominant tubulointerstitial kidney disease

ORPHA:34149Kr.
Autosomal dominant