Autosomal dominant spastic paraplegia type 13

Orpha code: 100994OMIM code: 605280

Definition

A rare, pure or complex form of hereditary spastic paraplegia characterized by progressive spastic paraplegia with pyramidal signs in the upper and lower limbs, and decreased vibration sense.

Disease data
Classification

Disease

Synonyms
SPG13
SPG13
ORPHA code
100994
OMIM code
605280
ICD10 code
G11.4
ICD11 code
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl