hereditary episodic ataxia
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
hereditary episodic ataxia
- episodic ataxia
disease_grouping, ordo_group_of_disorders
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
ea syndrome, episodic ataxia syndrome, Isaacs syndrome
MONDO:0016227
https://icd.codes/icd10cm/G11.8