Autosomal recessive cerebellar ataxia

Orpha code: 1172OMIM code:

Definition

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
Classification

Category

Synonyms
ARCA
ARCA
ORPHA code
1172
OMIM code
-
ICD10 code
-
ICD11 code
-

No additional description.

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