Impaired vibration sensation in the lower limbs

Symptom Information:

Symptom ID: HPO:0002166
Synonyms:
Decreased lower limb vibratory sense [HPO:0002166]
Decreased vibratory sense in lower limbs [HPO:0002166]
Decreased vibratory sense in the lower extremities [HPO:0002166]
Decreased vibratory sense in the lower limbs [HPO:0002166]
Diminished vibratory sensation in the legs [HPO:0002166]
Distal sensory loss, especially vibratory sense [HPO:0002166]
Distal vibratory impairment of the lower limbs [HPO:0002166]
Decreased lower limb vibratory sense [OMIM:Decreased lower limb vibratory sense]
Decreased vibratory sense in lower limbs [OMIM:Decreased vibratory sense in lower limbs]
Decreased vibratory sense in the lower extremities [OMIM:Decreased vibratory sense in the lower extremities]
Decreased vibratory sense in the lower limbs [OMIM:Decreased vibratory sense in the lower limbs]
Diminished vibratory sensation in the legs [OMIM:Diminished vibratory sensation in the legs]
Distal sensory loss, especially vibratory sense [OMIM:Distal sensory loss, especially vibratory sense]
Distal vibratory impairment of the lower limbs [OMIM:Distal vibratory impairment of the lower limbs]
Decreased vibratory sense in the lower limbs (in some patients) [OMIM:Decreased vibratory sense in the lower limbs (in some patients)]
Quality:
Cross references:
OMIM: "Decreased lower limb vibratory sense" [OMIM:Decreased lower limb vibratory sense]
OMIM: "Decreased vibratory sense in lower limbs" [OMIM:Decreased vibratory sense in lower limbs]
OMIM: "Decreased vibratory sense in the lower extremities" [OMIM:Decreased vibratory sense in the lower extremities]
OMIM: "Decreased vibratory sense in the lower limbs" [OMIM:Decreased vibratory sense in the lower limbs]
OMIM: "Diminished vibratory sensation in the legs" [OMIM:Diminished vibratory sensation in the legs]
OMIM: "Distal sensory loss, especially vibratory sense" [OMIM:Distal sensory loss, especially vibratory sense]
OMIM: "Distal vibratory impairment of the lower limbs" [OMIM:Distal vibratory impairment of the lower limbs]
OMIM: "Decreased vibratory sense in the lower limbs (in some patients)" [OMIM:Decreased vibratory sense in the lower limbs (in some patients)]
Is a (Direct Parents):
HPO         Impaired vibratory sensation
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:
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)