Torsion dystonia

Symptom Information:

Symptom ID: HPO:0001304
Synonyms:
Dystonia musculorum deformans [HPO:0001304]
Torsion dystonia [OMIM:Torsion dystonia]
Torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing) [OMIM:Torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing)]
Quality:
Cross references:
OMIM: "Torsion dystonia" [OMIM:Torsion dystonia]
OMIM: "Torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing)" [OMIM:Torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing)]
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)
                   Torsion dystonia(HPO:0001304)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant cervical dystonia (Orphanet:93962)
Autosomal dominant focal dystonia, DYT7 type (Orphanet:93963)
Blepharonasofacial malformation syndrome (Orphanet:1252)
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT (OMIM:128100)
DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE (OMIM:224500)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Early-onset generalized limb-onset dystonia (Orphanet:256)
Primary dystonia, DYT13 type (Orphanet:98807)
Primary dystonia, DYT2 type (Orphanet:99657)
Primary dystonia, DYT4 type (Orphanet:98805)
Primary dystonia, DYT6 type (Orphanet:98806)
TORSION DYSTONIA WITH ONSET IN INFANCY (OMIM:602554)
X-linked dystonia-parkinsonism (Orphanet:53351)