Terminology Service for NFDI4Health
hereditary ataxia
Go to external page
http://www.ebi.ac.uk/efo/EFO_0009671
An instance of an atactic disorder that is caused by an inherited genomic modification in an individual. [ ]
Term info
Label
hereditary ataxia
Synonyms
- hereditary ataxia
- rare hereditary ataxia
Subsets
gard_rare, disease_grouping, ordo_group_of_disorders
created by
https://orcid.org/0000-0001-5208-3432
exactMatch
http://identifiers.org/mesh/C531684, http://purl.obolibrary.org/obo/DOID_0050951, http://identifiers.org/snomedct/763597000, http://purl.obolibrary.org/obo/Orphanet_183518, https://icd.codes/icd10cm/G11
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0000437
id
EFO:0009671
see also
https://rarediseases.info.nih.gov/diseases/6614/hereditary-ataxia