Hyperkinesis

Symptom Information:

Symptom ID: HPO:0002487
Synonyms:
Hyperkinesia [HPO:0002487]
Hyperkinesia [Orphanet:43230]
Hyperkinesia [OMIM:Hyperkinesia]
Hyperkinesis [OMIM:Hyperkinesis]
Hyperkinesia/dyskinesia [Orphanet:43230]
Hyperkinesia [MedDRA:10020651]
Hyperkinesis [MedDRA:10020651]
Hyperkinetic reaction [MedDRA:10020651]
Quality:
Cross references:
Orphanet:43230 "Hyperkinesia/dyskinesia" [Orphanet:43230]
OMIM: "Hyperkinesia" [OMIM:Hyperkinesia]
OMIM: "Hyperkinesis" [OMIM:Hyperkinesis]
Is a (Direct Parents):
Orphanet Abnormality of movement
MedDRA Dyskinesias and movement disorders NEC
HPO         Abnormality of movement
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of movement(HPO:0100022)
                Hyperkinesis(HPO:0002487)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Dyskinesias and movement disorders NEC(MedDRA:10013929)
          Hyperkinesis(HPO:0002487)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

4-hydroxybutyric aciduria (Orphanet:22)
Christianson syndrome (Orphanet:85278)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Leigh syndrome (Orphanet:506)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
VALINEMIA (OMIM:277100)