A neurological syndrome characterized by clumsy and uncoordinated movement of the limbs, trunk, and cranial muscles. It results from pathology in the cerebellum and its connections, or in the proprioceptive sensory pathways. [ https://bestpractice.bmj.com/topics/en-gb/1097 ]
Synonyms: ataxia syndrome spinocerebellar Degeneration
Term information
- MEDGEN:849 (MONDO:equivalentTo)
- DOID:0050753 (MONDO:equivalentTo)
- MESH:D002524 (MONDO:equivalentTo)
- NANDO:1200037 (https://orcid.org/0000-0003-0011-764X)
- NCIT:C82341 (MONDO:equivalentTo)
- NANDO:2200882 (https://orcid.org/0000-0003-0011-764X)
- ICD9:334.3 (MONDO:relatedTo)
- UMLS:C0007758 (MONDO:equivalentTo)
- GARD:19816 (MONDO:GARD)
- SCTID:85102008 (MONDO:equivalentTo)
- Orphanet:102002 (MONDO:equivalentTo)
- NANDO:2100238 (https://orcid.org/0000-0003-0011-764X)
gard_rare, mondo_rare, otar, disease_grouping, rare, nord_rare, clingen, ordo_group_of_disorders
In ORDO this is called rare ataxia, we rename as ataxia since all forms are individually rare
http://purl.obolibrary.org/obo/DOID_0050753
http://linkedlifedata.com/resource/umls/id/C0007758
http://identifiers.org/snomedct/85102008
http://www.orpha.net/ORDO/Orphanet_102002
http://purl.obolibrary.org/obo/NCIT_C82341
http://identifiers.org/medgen/849
http://identifiers.org/mesh/D002524
ataxia
ataxias, cerebellar
ataxia, cerebellar
cerebellar Ataxias
rare ataxia
cerebellar Dysmetrias
cerebellar dysmetria
Term relations
- movement disorder
- cerebellar disorder
- atactic disorder
- disease has feature some Ataxia
- has characteristic some rare
- disease has basis in dysfunction of some cerebellum