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Autosomal dominant spastic paraplegia type 36
disorderSNOMED 723819007CUI C2936879
Overview
Autosomal dominant spastic paraplegia type 36 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.
Extensor plantar responses
Very frequent (80-99%)HP:0003487
Increased reflexes
Very frequent (80-99%)HP:0001347
Progressive spastic paraplegia
Very frequent (80-99%)HP:0007020
Spastic walk
Very frequent (80-99%)HP:0002064
Spasticity of lower limb
Very frequent (80-99%)HP:0002061
Decreased distal vibration sense
Frequent (30-79%)HP:0006886
Demyelinating motor neuropathy
Frequent (30-79%)HP:0007220
Demyelinating sensory neuropathy
Frequent (30-79%)HP:0011402
Impaired distal proprioception
Frequent (30-79%)HP:0006858
Impaired distal tactile sensation
Frequent (30-79%)HP:0006937
Impaired thermal sensitivity
Frequent (30-79%)HP:0010829
Proximal limb muscle weakness
Frequent (30-79%)HP:0003701
Urinary incontinence
Frequent (30-79%)HP:0000020
Urinary urgency
Frequent (30-79%)HP:0000012
Weakness of outermost muscles
Frequent (30-79%)HP:0002460
Arthritis
Occasional (5-29%)HP:0001369
Pes cavus
Occasional (5-29%)HP:0001761
Squint
Occasional (5-29%)HP:0000486
Distal sensory loss, especially vibratory sense
HP:0002166
Lower limb muscle weakness
HP:0007340
Sensory neuropathy
HP:0000763
Spastic paraplegia
HP:0001258
Related Conditions
Quick Facts
- SNOMED CT
- 723819007
- UMLS CUI
- C2936879
- Fully Specified Name
- Autosomal dominant spastic paraplegia type 36 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
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.