JSON

hereditary ataxia

^ 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 ]

Term info

database cross reference
  • Orphanet:183518 (MONDO:equivalentTo)
  • ICD10CM:G11 (MONDO:equivalentTo)
  • DOID:0050951 (MONDO:equivalentTo)
  • GARD:0010748 (MONDO:equivalentTo)
  • MESH:C531684 (MONDO:equivalentTo)
  • GARD:0006614 (MONDO:equivalentTo)
  • SCTID:763597000 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, ordo_group_of_disorders

abbreviation
SCA [ GARD:0010748 ]

created by

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

definition

An instance of an atactic disorder that is caused by an inherited genomic modification in an individual.

exactMatch

http://identifiers.org/mesh/C531684, http://purl.bioontology.org/ontology/ICD10CM/G11, http://purl.obolibrary.org/obo/DOID_0050951, http://identifiers.org/snomedct/763597000, http://purl.obolibrary.org/obo/Orphanet_183518

excluded subClassOf

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

has exact synonym

rare hereditary ataxia

id

MONDO:0100309

seeAlso

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