Resting tremor
Symptom Information:
Symptom ID: | HPO:0002322 | ||||
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) Tremor(HPO:0001337) Resting tremor(HPO:0002322) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Tremor(HPO:0001337) Resting tremor(HPO:0002322) |
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Database Frequency: | 14 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
Familial dyskinesia and facial myokymia | (Orphanet:324588) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
PARKINSON DISEASE 11, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | (OMIM:607688) |
PARKINSON DISEASE 17 | (OMIM:614203) |
PARKINSON DISEASE 18, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | (OMIM:614251) |
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:605909) |
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:606324) |
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT | (OMIM:607060) |
PARKINSON DISEASE, LATE-ONSET | (OMIM:168600) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
X-linked parkinsonism-spasticity syndrome | (Orphanet:363654) |
Young adult-onset Parkinsonism | (Orphanet:2828) |