Overview
Autosomal spastic paraplegia type 72 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.
Muscle rigidity
Very frequent (80-99%)HP:0002063
Spastic walk
Very frequent (80-99%)HP:0002064
Pes cavus
Frequent (30-79%)HP:0001761
Sphincter disturbances
Frequent (30-79%)HP:0002839
Abnormality of mental function
Occasional (5-29%)HP:0011446
Decreased vibration sense in feet
Occasional (5-29%)HP:0006938
Memory impairment
Occasional (5-29%)HP:0002354
Pain
Occasional (5-29%)HP:0012531
Postural tremor
Occasional (5-29%)HP:0002174
Quick Facts
- SNOMED CT
- 782727008
- UMLS CUI
- C3810160
- Fully Specified Name
- Autosomal spastic paraplegia type 72 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 9
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.