autosomal dominant cerebellar ataxia type III

Go to external page http://purl.obolibrary.org/obo/MONDO_0019793


Autosomal dominant cerebellar ataxia (ACDA) type III is a group of neurodegenerative disorders characterized by mostly pure cerebellar syndromes with occasional non-cerebellar signs (e.g. pyramidal signs, peripheral neuropathy, writer's cramp) and includes spinocerebellar ataxia (SCA) type 5 (SCA5), SCA6, SCA11, SCA26, SCA30, and SCA31. [ Orphanet:94148 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:G11.8 (Orphanet:94148)
  • UMLS:CN206746 (MONDO:equivalentTo)
  • Orphanet:94148 (MONDO:equivalentTo)
Subsets

ordo_group_of_disorders

abbreviation
ADCAIII [ Orphanet:94148 ]

abbreviation
ADCA3 [ Orphanet:94148 ]

definition

Autosomal dominant cerebellar ataxia (ACDA) type III is a group of neurodegenerative disorders characterized by mostly pure cerebellar syndromes with occasional non-cerebellar signs (e.g. pyramidal signs, peripheral neuropathy, writer's cramp) and includes spinocerebellar ataxia (SCA) type 5 (SCA5), SCA6, SCA11, SCA26, SCA30, and SCA31.

exactMatch

http://www.orpha.net/ORDO/Orphanet_94148

http://linkedlifedata.com/resource/umls/id/CN206746

has exact synonym

Pure cerebellar syndrome-mild pyramidal signs syndrome

ADCA3

ADCAIII

autosomal dominant cerebellar ataxia type 3

autosomal dominant cerebellar ataxia type III

id

MONDO:0019793

Term relations