Torsion dystonia
Symptom Information:
Symptom ID: | HPO:0001304 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |