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Autosomal recessive spastic paraplegia type 62
disorderSNOMED 765045003CUI C4284588
Overview
Autosomal recessive spastic paraplegia type 62 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.
Involuntary muscle stiffness, contraction, or spasm
Always present (100%)HP:0001257
Extensor plantar responses
Very frequent (80-99%)HP:0003487
Lower limb hyperreflexia
Very frequent (80-99%)HP:0002395
Spasticity of lower limb
Very frequent (80-99%)HP:0002061
Difficulty articulating speech
Frequent (30-79%)HP:0001260
Gait disturbance
Frequent (30-79%)HP:0001288
Increased reflexes
Frequent (30-79%)HP:0001347
Walking on tiptoes
Frequent (30-79%)HP:0030051
Absent patellar reflexes
Occasional (5-29%)HP:0006844
Ankle clonus
Occasional (5-29%)HP:0011448
Areflexia
Occasional (5-29%)HP:0001284
Cerebellar abnormality
Occasional (5-29%)HP:0001317
Clonus
Occasional (5-29%)HP:0002169
Inability to straighten knee
Occasional (5-29%)HP:0006380
Lower limb pain
Occasional (5-29%)HP:0012514
Muscle wasting
Occasional (5-29%)HP:0003202
Spastic walk
Occasional (5-29%)HP:0002064
Thoracic scoliosis
Occasional (5-29%)HP:0002943
Hoffmann's sign
Excluded (<1%)HP:0031993
Muscle fasciculation
Excluded (<1%)HP:0002380
Related Conditions
Quick Facts
- SNOMED CT
- 765045003
- UMLS CUI
- C4284588
- Fully Specified Name
- Autosomal recessive spastic paraplegia type 62 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.