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Autosomal recessive spastic paraplegia type 63
disorderSNOMED 726610000CUI C3810295
Overview
Autosomal recessive spastic paraplegia type 63 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.
Delayed ability to walk
Always present (100%)HP:0031936
Extensor plantar responses
Always present (100%)HP:0003487
Gait disturbance
Always present (100%)HP:0001288
Clonus
Frequent (30-79%)HP:0002169
Decreased body height
Frequent (30-79%)HP:0004322
Decreased vibration sense in feet
Frequent (30-79%)HP:0006938
Delayed gross motor development
Frequent (30-79%)HP:0002194
Hypoplasia of corpus callosum
Frequent (30-79%)HP:0002079
Increased reflexes
Frequent (30-79%)HP:0001347
Involuntary muscle stiffness, contraction, or spasm
Frequent (30-79%)HP:0001257
Low body weight
Frequent (30-79%)HP:0004325
Muscle degeneration
Frequent (30-79%)HP:0003202
Scissor gait
Frequent (30-79%)HP:0012407
Spasticity and rigidity of muscles
Frequent (30-79%)HP:0001276
Abnormality of the periventricular white matter
Occasional (5-29%)HP:0002518
Dull intelligence
Excluded (<1%)HP:0001249
Spastic paraplegia
HP:0001258
Quick Facts
- SNOMED CT
- 726610000
- UMLS CUI
- C3810295
- Fully Specified Name
- Autosomal recessive spastic paraplegia type 63 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
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.