Impaired distal vibration sensation
Symptom Information:
Symptom ID: | HPO:0006886 | ||
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 morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Peripheral neuropathy(HPO:0009830) Sensory impairment(HPO:0003474) Impaired vibratory sensation(HPO:0002495) Impaired distal vibration sensation(HPO:0006886) MedDRA: |
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Database Frequency: | 8 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2P | (Orphanet:300319) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |