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Autosomal recessive spastic paraplegia type 32
disorderSNOMED 726606003CUI C1970009
Overview
Autosomal recessive spastic paraplegia type 32 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.
Abnormal pons morphology
Frequent (30-79%)HP:0007361
Cerebellar cortex degeneration
Frequent (30-79%)HP:0008278
Distal sensory loss, especially vibratory sense
Frequent (30-79%)HP:0002166
Extensor plantar responses
Frequent (30-79%)HP:0003487
Lower limb hyperreflexia
Frequent (30-79%)HP:0002395
Progressive polyneuropathy
Frequent (30-79%)HP:0007133
Progressive spastic paraplegia
Frequent (30-79%)HP:0007020
Spasticity, progressive
Frequent (30-79%)HP:0002191
Specific learning disability
Frequent (30-79%)HP:0001328
Ankle clonus
HP:0011448
Cavus foot
HP:0001761
Cerebral atrophy
HP:0002059
Degeneration of cerebellum
HP:0001272
Gait disturbance
HP:0001288
Hypoplasia of corpus callosum
HP:0002079
Increased reflexes
HP:0001347
Lower limb muscle weakness
HP:0007340
Mental retardation, mild
HP:0001256
Spastic paraplegia
HP:0001258
Spastic walk
HP:0002064
Spasticity of lower limb
HP:0002061
Quick Facts
- SNOMED CT
- 726606003
- UMLS CUI
- C1970009
- Fully Specified Name
- Autosomal recessive spastic paraplegia type 32 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 21
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.