Writer's cramp
Symptom Information:
Symptom ID: | HPO:0002356 | ||||||||
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) Focal dystonia(HPO:0004373) Writer's cramp(HPO:0002356) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Dystonias(MedDRA:10013985) Writer's cramp(HPO:0002356) |
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Database Frequency: | 16 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Autosomal dominant cervical dystonia | (Orphanet:93962) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT | (OMIM:128100) |
DYSTONIA 15, MYOCLONIC | (OMIM:607488) |
DYSTONIA 23 | (OMIM:614860) |
Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
Early-onset generalized limb-onset dystonia | (Orphanet:256) |
Limb dystonia | (Orphanet:93957) |
MELAS | (Orphanet:550) |
Myoclonus-dystonia syndrome | (Orphanet:36899) |
Neuroferritinopathy | (Orphanet:157846) |
Niemann-Pick disease type C | (Orphanet:646) |
Primary dystonia, DYT13 type | (Orphanet:98807) |
Primary dystonia, DYT6 type | (Orphanet:98806) |
Rolandic epilepsy - paroxysmal exercise-induced dystonia - writer's cramp | (Orphanet:163727) |