Hyperkinetic movements

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Hyperkinetic movements" [OMIM:Hyperkinetic movements]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive limb-girdle muscular dystrophy type 2S (Orphanet:369840)
Christianson syndrome (Orphanet:85278)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)