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Autosomal dominant familial spastic paraplegia type 3
disorderSNOMED 732949006CUI C1838192
Overview
Autosomal dominant familial spastic paraplegia type 3 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
Gait disturbance
Very frequent (80-99%)HP:0001288
Impaired vibratory sensation
Very frequent (80-99%)HP:0002495
Lower limb hyperreflexia
Very frequent (80-99%)HP:0002395
Spasticity of lower limb
Very frequent (80-99%)HP:0002061
Cavus foot
Frequent (30-79%)HP:0001761
Generalized tonic-clonic seizure (without specification of onset)
Frequent (30-79%)HP:0002069
Limitation of movement at ankles
Frequent (30-79%)HP:0010505
Limited hip movement
Frequent (30-79%)HP:0008800
Muscle atrophy, neurogenic
Frequent (30-79%)HP:0003202
Postural tremor
Occasional (5-29%)HP:0002174
Tremor
Occasional (5-29%)HP:0001337
Urinary incontinence
Occasional (5-29%)HP:0000020
Clonus
HP:0002169
Degeneration of the lateral corticospinal tracts
HP:0002314
Distal sensory loss, especially vibratory sense
HP:0002166
Increased reflexes
HP:0001347
Lower limb muscle weakness
HP:0007340
Seizures
HP:0001250
Spastic paraplegia
HP:0001258
Spastic walk
HP:0002064
Sphincter disturbances
HP:0002839
Urinary urgency
HP:0000012
Related Conditions
Quick Facts
- SNOMED CT
- 732949006
- UMLS CUI
- C1838192
- Fully Specified Name
- Autosomal dominant spastic paraplegia type 6 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 23
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.