Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Friedreich's ataxia
Frequent (30-79%)
Ehlers-Danlos syndrome, hydroxylysine-deficient
Occasional (5-29%)
Chorea acanthocytosis syndrome
Frequent (30-79%)
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Roussy-Lévy syndrome
Frequent (30-79%)
Acute transverse myelitis
Occasional (5-29%)
Azorean disease
Hereditary sensory and autonomic neuropathy, type V
Frequent (30-79%)
ABL - Abetalipoproteinaemia
Occasional (5-29%)
Troyer syndrome
Frequent (30-79%)
Senile systemic amyloidosis
Frequent (30-79%)
Chylomicron retention disease
ARSACS - autosomal recessive spastic ataxia of Charlevoix-Saguenay
Occasional (5-29%)
Spinocerebellar ataxia type 1
Always present (100%)
Spinocerebellar ataxia type 2
Spinocerebellar ataxia type 8
Occasional (5-29%)
Spinocerebellar ataxia type 4
Very frequent (80-99%)
Charcot-Marie-Tooth disease type 4G
Very frequent (80-99%)
Spinocerebellar ataxia type 31
Occasional (5-29%)
Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
Frequent (30-79%)
Spinocerebellar ataxia type 27
Frequent (30-79%)
Spinocerebellar ataxia type 5
Charcot-Marie-Tooth disease type IF
Frequent (30-79%)
Autosomal recessive spastic paraplegia type 46
Occasional (5-29%)
Autosomal recessive spastic paraplegia type 53
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 130980003
- UMLS CUI
- C1295585
- Fully Specified Name
- Decreased vibratory sense (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.