Akinesia

Symptom Information:

Symptom ID: HPO:0002304
Synonyms:
Akinesia (finding) [Orphanet:43320]
Akinesia [Orphanet:43320]
Akinesia [OMIM:Akinesia]
Execution movement disorder/dysmetria/bradykinesia/akinesia/apraxia [Orphanet:43320]
Akinesia [MedDRA:10001541]
Execution movement disorder [Orphanet:43320]
Quality:
Cross references:
Orphanet:43320 "Execution movement disorder/dysmetria/bradykinesia/akinesia/apraxia" [Orphanet:43320]
OMIM: "Akinesia" [OMIM:Akinesia]
UMLS:C0085623 "Akinesia" [HPO:0002304]
UMLS:C0085623 "Akinesia" [Orphanet:43320]
Is a (Direct Parents):
Orphanet Dysmetria
Orphanet [DEL]Motor deficit/trouble
HPO         Diminished movement
MedDRA Dyskinesias and movement disorders NEC
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)
                Diminished movement(HPO:0002374)
                   Akinesia(HPO:0002304)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Dyskinesias and movement disorders NEC(MedDRA:10013929)
          Akinesia(HPO:0002304)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Aceruloplasminemia (Orphanet:48818)
Classical progressive supranuclear palsy (Orphanet:240071)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Fetal Gaucher disease (Orphanet:85212)
Gaucher disease type 2 (Orphanet:77260)
HERNS syndrome (Orphanet:63261)
Huntington disease (Orphanet:399)
Kufor-Rakeb syndrome (Orphanet:306674)
Lethal congenital contracture syndrome type 2 (Orphanet:137776)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lissencephaly type 3 - metacarpal bone dysplasia (Orphanet:86822)
PARKINSON DISEASE 17 (OMIM:614203)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 (OMIM:601104)
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 (OMIM:609454)
Spinocerebellar ataxia type 21 (Orphanet:98773)
Tako-Tsubo cardiomyopathy (Orphanet:66529)