Preferred Name

autosomal dominant cerebellar ataxia

Synonyms

cerebellar ataxia, autosomal dominant

autosomal dominant spinocerebellar ataxia

ADCA

SCA

spinocerebellar ataxia

Pierre Marie cerebellar ataxia (formerly)

Definitions

A clinically and genetically heterogeneous group of neurodegenerative diseases characterized by a slowly progressive ataxia of gait, stance and limbs, dysarthria and/or oculomotor disorder, due to cerebellar degeneration in the absence of coexisting diseases. The degenerative process can be limited to the cerebellum (ADCA type 3) or may additionally involve the retina (ADCA type 2), optic nerve, ponto-medullary systems, basal ganglia, cerebral cortex, spinal tracts or peripheral nerves (ADCA type 1). In ACDA type 4, a cerebellar syndrome is associated with epilepsy.

ID

http://purl.obolibrary.org/obo/MONDO_0020380

disease has major feature

http://purl.obolibrary.org/obo/MONDO_0001627

has_broad_synonym

SCA

spinocerebellar ataxia

has_exact_synonym

cerebellar ataxia, autosomal dominant

autosomal dominant spinocerebellar ataxia

ADCA

has_related_synonym

Pierre Marie cerebellar ataxia (formerly)

IAO_0000233

https://github.com/monarch-initiative/mondo/pull/2571/

label

autosomal dominant cerebellar ataxia

prefixIRI

MONDO:0020380

prefLabel

autosomal dominant cerebellar ataxia

textual definition

A clinically and genetically heterogeneous group of neurodegenerative diseases characterized by a slowly progressive ataxia of gait, stance and limbs, dysarthria and/or oculomotor disorder, due to cerebellar degeneration in the absence of coexisting diseases. The degenerative process can be limited to the cerebellum (ADCA type 3) or may additionally involve the retina (ADCA type 2), optic nerve, ponto-medullary systems, basal ganglia, cerebral cortex, spinal tracts or peripheral nerves (ADCA type 1). In ACDA type 4, a cerebellar syndrome is associated with epilepsy.

subClassOf

http://purl.obolibrary.org/obo/MONDO_0022687

http://purl.obolibrary.org/obo/MONDO_0000426

http://purl.obolibrary.org/obo/MONDO_0024237

http://purl.obolibrary.org/obo/MONDO_0015547

http://purl.obolibrary.org/obo/MONDO_0100310

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