Overview
Autosomal dominant sensory neuropathy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Cataract
Always present (100%)HP:0000518
Decreased motor nerve conduction velocity
Always present (100%)HP:0003431
Frequent falls
Always present (100%)HP:0002359
Impaired distal proprioception
Always present (100%)HP:0006858
Muscle degeneration
Always present (100%)HP:0003202
Tongue fasciculations/fibrillations
Always present (100%)HP:0001308
tremors in hands
Always present (100%)HP:0002378
Abnormality of balance
Very frequent (80-99%)HP:0002141
Abnormality of the autonomic nervous system
Very frequent (80-99%)HP:0002270
Decreased amplitude of sensory action potentials
Very frequent (80-99%)HP:0007078
Impaired ability to dress oneself
Very frequent (80-99%)HP:0031060
Loss of distal sensation
Very frequent (80-99%)HP:0002936
Muscle weakness
Very frequent (80-99%)HP:0001324
Absence of pain sensation
Frequent (30-79%)HP:0007021
Epidermal hyperkeratosis
Frequent (30-79%)HP:0000962
Hypohidrosis or hyperhidrosis
Frequent (30-79%)HP:0007550
Impaired distal tactile sensation
Frequent (30-79%)HP:0006937
Impaired thermal sensitivity
Frequent (30-79%)HP:0010829
Inability to heel walk
Frequent (30-79%)HP:0009027
Limb pain
Frequent (30-79%)HP:0009763
Open skin sore
Frequent (30-79%)HP:0200042
Penetrating foot ulcers
Frequent (30-79%)HP:0001026
Poor wound healing
Frequent (30-79%)HP:0001058
Steppage gait
Frequent (30-79%)HP:0003376
Trophic changes
Frequent (30-79%)HP:0010834
Weakness of outermost muscles
Frequent (30-79%)HP:0002460
Charcot joint
Occasional (5-29%)HP:0002821
Coughing
Occasional (5-29%)HP:0012735
Distal muscle atrophy, upper and lower limbs
Occasional (5-29%)HP:0003693
EMG: slow motor conduction
Occasional (5-29%)HP:0100287
Quick Facts
- SNOMED CT
- 230553002
- UMLS CUI
- C0020071
- Fully Specified Name
- Autosomal dominant sensory neuropathy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.