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autosomal recessive cerebellar ataxia
Disease Summary
Associated Targets (129)
Tbio
104
Tchem
16
Tclin
5
Tdark
4
Mondo Description Autosomal recessive cerebellar ataxias (ARCA) are 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 Ontology Description A hereditary ataxia that has_material_basis_in autosomal recessive inheritance.
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0050950
OMIMPS:213200
Orphanet:1172
UMLS:CN226644
MONDO:0015244
High level summary of knowledge for a disease, including descriptions and datasource references. Click the "?" for more details.