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hereditary ataxia

Go to external page http://purl.obolibrary.org/obo/MONDO_0100309

An instance of an atactic disorder that is caused by an inherited genomic modification in an individual. [ MONDO:patterns/hereditary ]

Synonyms: rare hereditary ataxia

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10CM:G11 (MONDO:equivalentTo)
  • EFO:0009671 (MONDO:equivalentTo)
  • GARD:20286 (MONDO:GARD)
  • DOID:0050951 (MONDO:equivalentTo)
  • UMLS:C0004138 (MONDO:equivalentTo)
  • SCTID:763597000 (MONDO:equivalentTo)
  • MESH:C531684 (MONDO:equivalentTo)
  • MEDGEN:2478 (MONDO:equivalentTo)
  • Orphanet:183518 (MONDO:equivalentTo)
Subsets

gard_rare, mondo_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders

abbreviation
SCA [ GARD:0010748 ]

creator

https://orcid.org/0000-0001-5208-3432

exactMatch

http://identifiers.org/mesh/C531684

http://purl.bioontology.org/ontology/ICD10CM/G11

http://linkedlifedata.com/resource/umls/id/C0004138

http://purl.obolibrary.org/obo/DOID_0050951

http://www.orpha.net/ORDO/Orphanet_183518

http://identifiers.org/snomedct/763597000

http://identifiers.org/medgen/2478

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0000437

id

MONDO:0100309

seeAlso

https://rarediseases.info.nih.gov/diseases/6614/hereditary-ataxia