Cogwheel rigidity
Symptom Information:
Symptom ID: | HPO:0002396 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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 central motor function(HPO:0011442) Rigidity(HPO:0002063) Cogwheel rigidity(HPO:0002396) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Parkinson's disease and parkinsonism(MedDRA:10034005) Cogwheel rigidity(HPO:0002396) |
||||
Database Frequency: | 6 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
Spinocerebellar ataxia type 19/22 | (Orphanet:98772) |
Spinocerebellar ataxia type 21 | (Orphanet:98773) |
X-linked parkinsonism-spasticity syndrome | (Orphanet:363654) |