Rank (Similarity) |
PMID (PMCID) |
---|
|
Total: 11
HPO ID | Term | Frequency |
---|---|---|
HP:0001260 | Dysarthria | Very frequent (99-80%) |
HP:0001324 | Muscle weakness | Very frequent (99-80%) |
HP:0002131 | Episodic ataxia | Very frequent (99-80%) |
HP:0002321 | Vertigo | Very frequent (99-80%) |
HP:0000639 | Nystagmus | Frequent (79-30%) |
HP:0000360 | Tinnitus | Occasional (29-5%) |
HP:0000651 | Diplopia | Occasional (29-5%) |
HP:0002076 | Migraine | Occasional (29-5%) |
HP:0002411 | Myokymia | Occasional (29-5%) |
HP:0002487 | Hyperkinesis | Occasional (29-5%) |
HP:0100543 | Cognitive impairment | Occasional (29-5%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|