Autosomal recessive spastic paraplegia type 32

disorder

SNOMED 726606003CUI C1970009

Overview

Autosomal recessive spastic paraplegia type 32 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 pons morphology

Frequent (30-79%)HP:0007361

Cerebellar cortex degeneration

Frequent (30-79%)HP:0008278

Distal sensory loss, especially vibratory sense

Frequent (30-79%)HP:0002166

Extensor plantar responses

Frequent (30-79%)HP:0003487

Lower limb hyperreflexia

Frequent (30-79%)HP:0002395

Progressive polyneuropathy

Frequent (30-79%)HP:0007133

Progressive spastic paraplegia

Frequent (30-79%)HP:0007020

Spasticity, progressive

Frequent (30-79%)HP:0002191

Specific learning disability

Frequent (30-79%)HP:0001328

Ankle clonus

HP:0011448

Cavus foot

HP:0001761

Degeneration of cerebrum

HP:0002059

Gait disturbance

HP:0001288

Hypoplasia of corpus callosum

HP:0002079

Increased reflexes

HP:0001347

Infratentorial atrophy

HP:0001272

Lower limb muscle weakness

HP:0007340

Mental retardation, mild

HP:0001256

Spastic paraplegia

HP:0001258

Spastic walk

HP:0002064

Spasticity of lower limb

HP:0002061

Related Conditions

Complicated hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 726606003
UMLS CUI: C1970009
Fully Specified Name: Autosomal recessive spastic paraplegia type 32 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 21

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.