Overview
Autosomal spastic paraplegia type 30 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
Leg muscle stiffness
Very frequent (80-99%)HP:0008969
Lower limb hyperreflexia
Very frequent (80-99%)HP:0002395
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
Unsteady walk
Very frequent (80-99%)HP:0002317
Abnormal finger chase test
Frequent (30-79%)HP:0001310
Abnormal saccadic eye movements
Frequent (30-79%)HP:0000570
Ataxia
Frequent (30-79%)HP:0001251
Distal muscle atrophy, upper and lower limbs
Frequent (30-79%)HP:0003693
Loss of distal sensation
Frequent (30-79%)HP:0002936
Lower limb amyotrophy
Frequent (30-79%)HP:0007210
Lower limb muscle weakness
Frequent (30-79%)HP:0007340
Nerve damage causing decreased feeling and movement
Frequent (30-79%)HP:0007141
Peripheral axonal neuropathy
Frequent (30-79%)HP:0003477
Scissor gait
Frequent (30-79%)HP:0012407
Sensory impairment
Frequent (30-79%)HP:0003474
Diffuse cerebellar atrophy
Occasional (5-29%)HP:0100275
Ankle clonus
HP:0011448
Increased reflexes
HP:0001347
Infratentorial atrophy
HP:0001272
Spastic paraplegia
HP:0001258
Sphincter disturbances
HP:0002839
Quick Facts
- SNOMED CT
- 763377006
- UMLS CUI
- C5235139
- Fully Specified Name
- Autosomal spastic paraplegia type 30 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 24
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.