Postural tremor
Symptom Information:
Symptom ID: | HPO:0002174 | ||||||
Synonyms: |
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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) Tremor(HPO:0001337) Postural tremor(HPO:0002174) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Tremor(HPO:0001337) Postural tremor(HPO:0002174) |
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Database Frequency: | 22 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 8 | (OMIM:608627) |
Action myoclonus - renal failure syndrome | (Orphanet:163696) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:300619) |
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia | (Orphanet:284324) |
Dystonia 16 | (Orphanet:210571) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Leber hereditary optic neuropathy | (Orphanet:104) |
Leber plus disease | (Orphanet:99718) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
Odontoleukodystrophy | (Orphanet:77295) |
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:606324) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
Spinocerebellar ataxia type 15/16 | (Orphanet:98769) |
Spinocerebellar ataxia type 19/22 | (Orphanet:98772) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 20 | (Orphanet:101110) |
Spinocerebellar ataxia type 21 | (Orphanet:98773) |
Spinocerebellar ataxia type 27 | (Orphanet:98764) |
TREMOR, HEREDITARY ESSENTIAL, 1 | (OMIM:190300) |
TREMOR, HEREDITARY ESSENTIAL, 4 | (OMIM:614782) |
[DEL] LEBER OPTIC ATROPHY | (OMIM:535000) |