Limb dystonia

Symptom Information:

Symptom ID: HPO:0002451
Synonyms:
Limb dystonia [OMIM:Limb dystonia]
Limb dystonia (18%) [OMIM:Limb dystonia (18%)]
Quality:
Cross references:
OMIM: "Limb dystonia" [OMIM:Limb dystonia]
OMIM: "Limb dystonia (18%)" [OMIM:Limb dystonia (18%)]
Is a (Direct Parents):
HPO         Dystonia
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)
                Dystonia(HPO:0001332)
                   Limb dystonia(HPO:0002451)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Alpha-mannosidosis (Orphanet:61)
Aromatic L-amino acid decarboxylase deficiency (Orphanet:35708)
Autosomal dominant focal dystonia, DYT25 (Orphanet:329466)
Autosomal recessive dopa-responsive dystonia (Orphanet:101150)
Classical progressive supranuclear palsy (Orphanet:240071)
DYSTONIA 23 (OMIM:614860)
Dystonia 16 (Orphanet:210571)
Infantile dystonia-parkinsonism (Orphanet:238455)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
PORENCEPHALY 1 (OMIM:175780)
Partington syndrome (Orphanet:94083)
Porencephaly (Orphanet:2940)
Primary dystonia, DYT13 type (Orphanet:98807)
Primary dystonia, DYT4 type (Orphanet:98805)
Primary dystonia, DYT6 type (Orphanet:98806)
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 (OMIM:601104)