Facial-faucial-finger mini-myoclonus (FFF)
Symptom Information:
Symptom ID: | OMIM : No Id available | |
Synonyms: |
|
|
Quality: | ||
Cross references: |
|
|
Is a (Direct Parents): |
|
|
Is a (Whole tree): |
HPO:
MedDRA: |
|
Database Frequency: | 2 / 7739 | |
Resource: |
All diseases associated with this symptom:
Kufor-Rakeb syndrome | (Orphanet:306674) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |