Facial-faucial-finger mini-myoclonus (FFF)

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Facial-faucial-finger mini-myoclonus (FFF)" [OMIM:Facial-faucial-finger mini-myoclonus (FFF)]
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)