Spinocerebellar ataxia type 31 (SCA31) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the late-onset of cerebral ataxia, dysarthria and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense and hearing difficulties. [ Orphanet:217012 ]

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:0050980 (MONDO:equivalentTo)
  • ICD10:G11.8 (Orphanet:217012)
  • MESH:C566146 (MONDO:equivalentTo)
  • UMLS:C1861736 (Orphanet:217012)
  • UMLS:C4274986 (MONDO:equivalentTo)
  • SCTID:715826005 (MONDO:equivalentTo)
  • OMIM:117210 (Orphanet:217012)
  • GARD:0009975 (Orphanet-shared)
  • Orphanet:217012 (OMIM:117210)
Subsets

ordo_disease

abbreviation
SCA31 [ Orphanet:217012 https://omim.org/entry/117210 MONDO:Lexical ]

definition

Spinocerebellar ataxia type 31 (SCA31) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by the late-onset of cerebral ataxia, dysarthria and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense and hearing difficulties.

exactMatch

http://www.orpha.net/ORDO/Orphanet_217012

http://linkedlifedata.com/resource/umls/id/C4274986

http://linkedlifedata.com/resource/umls/id/C1861736

http://purl.obolibrary.org/obo/DOID_0050980

http://identifiers.org/snomedct/715826005

http://identifiers.org/omim/117210

http://identifiers.org/mesh/C566146

has exact synonym

spinocerebellar ataxia type 31

SCA31

has related synonym

spinocerebellar ataxia 16q22-linked

spinocerebellar ataxia, 16Q22-linked

spinocerebellar ataxia 31

id

MONDO:0007296