Akinesia
Symptom Information:
Symptom ID: | HPO:0002304 | ||||||||
Synonyms: |
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Quality: | |||||||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |