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Autosomal recessive spastic paraplegia type 67
disorderSNOMED 766767001CUI C4707829
Overview
Autosomal recessive spastic paraplegia type 67 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 myelination
Frequent (30-79%)HP:0012447
Abnormality of movement
Frequent (30-79%)HP:0100022
Absence of corpus callosum
Frequent (30-79%)HP:0001274
Cerebral cortex atrophy
Frequent (30-79%)HP:0002120
Cognitive delay
Frequent (30-79%)HP:0001263
Extensor plantar responses
Frequent (30-79%)HP:0003487
Gait disturbance
Frequent (30-79%)HP:0001288
Hypo/aplastic vermis
Frequent (30-79%)HP:0006817
Increased reflexes
Frequent (30-79%)HP:0001347
Limb tremor
Frequent (30-79%)HP:0200085
Mental retardation, mild
Frequent (30-79%)HP:0001256
Muscle atrophy, generalised
Frequent (30-79%)HP:0003700
Progressive spastic paraplegia
Frequent (30-79%)HP:0007020
Spastic walk
Frequent (30-79%)HP:0002064
Spasticity of lower limb
Frequent (30-79%)HP:0002061
Quick Facts
- SNOMED CT
- 766767001
- UMLS CUI
- C4707829
- Fully Specified Name
- Autosomal recessive spastic paraplegia type 67 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 15
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.