Autosomal recessive spastic paraplegia type 59

disorder

SNOMED 773425000CUI C4750857

Overview

Autosomal recessive spastic paraplegia type 59 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.

Spastic paraplegia

Very frequent (80-99%)HP:0001258

Appendicular hypertonia

Frequent (30-79%)HP:0002509

Clonus

Frequent (30-79%)HP:0002169

Fetal foot inversion

Frequent (30-79%)HP:0001762

Involuntary, rapid, rhythmic eye movements

Frequent (30-79%)HP:0000639

Lower limb hyperreflexia

Frequent (30-79%)HP:0002395

Spastic walk

Frequent (30-79%)HP:0002064

Spasticity of lower limb

Frequent (30-79%)HP:0002061

Dull intelligence

Occasional (5-29%)HP:0001249

Related Conditions

Complicated hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 773425000
UMLS CUI: C4750857
Fully Specified Name: Autosomal recessive spastic paraplegia type 59 (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.