Autosomal recessive spastic paraplegia type 71

disorder

SNOMED 782726004CUI C5190578

Overview

Autosomal recessive spastic paraplegia type 71 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

Extensor plantar responses

Frequent (30-79%)HP:0003487

Hypoplasia of corpus callosum

Frequent (30-79%)HP:0002079

Increased reflexes

Frequent (30-79%)HP:0001347

Mental and motor retardation

Frequent (30-79%)HP:0001263

Mental retardation, mild

Frequent (30-79%)HP:0001256

Peripheral neuropathy

Frequent (30-79%)HP:0009830

Progressive spastic paraplegia

Frequent (30-79%)HP:0007020

Spastic walk

Frequent (30-79%)HP:0002064

Spasticity of lower limb

Frequent (30-79%)HP:0002061

tremors in hands

Frequent (30-79%)HP:0002378

Related Conditions

Pure hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 782726004
UMLS CUI: C5190578
Fully Specified Name: Autosomal recessive spastic paraplegia type 71 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.