Limb dystonia
Symptom Information:
Symptom ID: | HPO:0002451 | ||
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) Limb dystonia(HPO:0002451) MedDRA: |
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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) |