Focal dystonia

Symptom Information:

Symptom ID: HPO:0004373
Synonyms:
Dystonia, focal [OMIM:Dystonia, focal]
Dystonia, focal (at onset) [OMIM:Dystonia, focal (at onset)]
Focal dystonia (adult onset) [OMIM:Focal dystonia (adult onset)]
Focal dystonia (e.g., writer's cramp) [OMIM:Focal dystonia (e.g., writer's cramp)]
Focal dystonia (rare) [OMIM:Focal dystonia (rare)]
Quality:
Cross references:
OMIM: "Dystonia, focal" [OMIM:Dystonia, focal]
OMIM: "Dystonia, focal (at onset)" [OMIM:Dystonia, focal (at onset)]
OMIM: "Focal dystonia (adult onset)" [OMIM:Focal dystonia (adult onset)]
OMIM: "Focal dystonia (e.g., writer's cramp)" [OMIM:Focal dystonia (e.g., writer's cramp)]
OMIM: "Focal dystonia (rare)" [OMIM:Focal dystonia (rare)]
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)
                   Focal dystonia(HPO:0004373)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant dopa-responsive dystonia (Orphanet:98808)
Autosomal dominant focal dystonia, DYT25 (Orphanet:329466)
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT (OMIM:128100)
DYSTONIA 24 (OMIM:615034)
DYSTONIA WITH CEREBELLAR ATROPHY (OMIM:611694)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Neuroferritinopathy (Orphanet:157846)
Partington syndrome (Orphanet:94083)
Spinocerebellar ataxia type 14 (Orphanet:98763)