Impaired vibratory sensation

Symptom Information:

Symptom ID: HPO:0002495
Synonyms:
Decreased vibration sense [HPO:0002495]
Decreased vibratory sense [HPO:0002495]
Diminished vibratory sense [HPO:0002495]
Impaired vibratory sense [HPO:0002495]
Decreased vibration sense [OMIM:Decreased vibration sense]
Diminished vibratory sense [OMIM:Diminished vibratory sense]
Impaired vibratory sense [OMIM:Impaired vibratory sense]
Decreased vibration sense (rare) [OMIM:Decreased vibration sense (rare)]
Decreased vibratory sense (less common) [OMIM:Decreased vibratory sense (less common)]
Decreased vibratory sense [MedDRA:10067502]
Quality:
Cross references:
OMIM: "Decreased vibration sense" [OMIM:Decreased vibration sense]
OMIM: "Diminished vibratory sense" [OMIM:Diminished vibratory sense]
OMIM: "Impaired vibratory sense" [OMIM:Impaired vibratory sense]
OMIM: "Decreased vibration sense (rare)" [OMIM:Decreased vibration sense (rare)]
OMIM: "Decreased vibratory sense (less common)" [OMIM:Decreased vibratory sense (less common)]
Is a (Direct Parents):
HPO         Sensory impairment
MedDRA Sensory abnormalities NEC
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)
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)