Impaired vibratory sensation
Symptom Information:
Symptom ID: | HPO:0002495 | ||||||||||
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) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Sensory abnormalities NEC(MedDRA:10040021) Impaired vibratory sensation(HPO:0002495) |
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Database Frequency: | 26 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 29 | (Orphanet:101009) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia | (Orphanet:284324) |
Chronic intestinal pseudo-obstruction | (Orphanet:2978) |
Chylomicron retention disease | (Orphanet:71) |
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
Friedreich ataxia 1 | (OMIM:229300) |
Friedreich ataxia 2 | (OMIM:601992) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Leber plus disease | (Orphanet:99718) |
POSTERIOR COLUMN ATAXIA | (OMIM:176250) |
Spastic paraplegia 64, autosomal recessive | (OMIM:615683) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 27 | (Orphanet:98764) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Spinocerebellar ataxia type 5 | (Orphanet:98766) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked spastic paraplegia type 34 | (Orphanet:171607) |