Upper limb spasticity

Symptom Information:

Symptom ID: HPO:0006986
Synonyms:
Upper limb spasticity [OMIM:Upper limb spasticity]
Upper limb spasticity (some) [OMIM:Upper limb spasticity (some)]
Quality:
Cross references:
OMIM: "Upper limb spasticity" [OMIM:Upper limb spasticity]
OMIM: "Upper limb spasticity (some)" [OMIM:Upper limb spasticity (some)]
Is a (Direct Parents):
HPO         Spasticity
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)