Autosomal recessive cerebellar ataxia

Orpha code: 1172OMIM code:

Definicja

A heterogeneous group of rare neurological disorders involving both the central and peripheral nervous system (and in some cases other systems and organs), and characterized by degeneration or abnormal development of the cerebellum and spinal cord and, in most cases, early onset occurring before the age of 20 years.

Disease data
Klasyfikacja

Category

Synonimy
ARCA
ARCA
Kod ORPHA
1172
Kod OMIM
-
Kod ICD10
-
Kod ICD11
-

No additional description.

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