Autosomal recessive spastic paraplegia type 39

disorder

SNOMED 719103009CUI C2677586

Overview

Autosomal recessive spastic paraplegia type 39 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.

Degeneration of the spinal cord

Frequent (30-79%)HP:0006827

Extensor plantar responses

Frequent (30-79%)HP:0003487

Generalised muscle wasting

Frequent (30-79%)HP:0009055

Length dependent motor neuropathy

Frequent (30-79%)HP:0007002

Spastic paraplegia

Frequent (30-79%)HP:0001258

Spasticity of lower limb

Frequent (30-79%)HP:0002061

Ataxia

Occasional (5-29%)HP:0001251

Degeneration of cerebellum

Occasional (5-29%)HP:0001272

Inability to coordinate movements when walking

Occasional (5-29%)HP:0002066

Distal muscle atrophy, upper and lower limbs

HP:0003693

Distal muscle weakness in lower limbs

HP:0009053

Gait disturbance

HP:0001288

Increased reflexes

HP:0001347

Progressive spastic paraplegia

HP:0007020

Related Conditions

Complicated hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 719103009
UMLS CUI: C2677586
Fully Specified Name: Autosomal recessive spastic paraplegia type 39 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.