Terminology Service for NFDI4Health

hereditary episodic ataxia

Go to external page http://purl.obolibrary.org/obo/MONDO_0016227


Hereditary episodic ataxia (EA) represents a group of neurological disorders characterized by recurrent episodes of ataxia and vertigo which may be progressive. Weakness, dystonia and ataxia are sometimes present in the interictal period. Seven types of EA have been described to date (EA type 1 to EA type 7), but most of the reported cases belong to EA1 and EA2. [ ]

Term info

Label

hereditary episodic ataxia

Synonyms
  • episodic ataxia
database cross reference
Subsets

disease_grouping, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/Orphanet_211062, http://linkedlifedata.com/resource/umls/id/C1720189, https://omim.org/phenotypicSeries/PS160120, http://identifiers.org/snomedct/421455009, http://purl.obolibrary.org/obo/DOID_963

has related synonym

ea syndrome, episodic ataxia syndrome, Isaacs syndrome

id

MONDO:0016227

narrowMatch

https://icd.codes/icd10cm/G11.8

Term relations

Subclass of: