Impaired vibration sensation in the lower limbs
Symptom Information:
Symptom ID: | HPO:0002166 | |||||||||||||||
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 vibration sensation in the lower limbs(HPO:0002166) MedDRA: |
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Database Frequency: | 26 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
Ataxia - pancytopenia | (Orphanet:2585) |
Autosomal dominant optic atrophy plus syndrome | (Orphanet:1215) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 12 | (Orphanet:100993) |
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 17 | (Orphanet:100998) |
Autosomal dominant spastic paraplegia type 19 | (Orphanet:100999) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal dominant spastic paraplegia type 36 | (Orphanet:320365) |
Autosomal dominant spastic paraplegia type 37 | (Orphanet:171612) |
Autosomal dominant spastic paraplegia type 38 | (Orphanet:171617) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal dominant spastic paraplegia type 8 | (Orphanet:100989) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 5A | (Orphanet:100986) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Friedreich ataxia 2 | (OMIM:601992) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION | (OMIM:607565) |
Spinocerebellar ataxia type 23 | (Orphanet:101108) |
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE | (OMIM:607259) |