Upper limb spasticity
Symptom Information:
Symptom ID: | HPO:0006986 | ||
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) Abnormal pyramidal signs(HPO:0007256) Hypertonia(HPO:0001276) Spasticity(HPO:0001257) Upper limb spasticity(HPO:0006986) MedDRA: |
||
Database Frequency: | 15 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant spastic paraplegia type 29 | (Orphanet:101009) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 37 | (Orphanet:171612) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal dominant spastic paraplegia type 8 | (Orphanet:100989) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 18 | (Orphanet:209951) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 44 | (Orphanet:320401) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |