Autosomal dominant spastic paraplegia type 41

disorder

SNOMED 763069002CUI C3888208

Overview

Autosomal dominant spastic paraplegia type 41 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 lateral corticospinal tracts

Very frequent (80-99%)HP:0002314

Progressive spastic paraplegia

Very frequent (80-99%)HP:0007020

Spastic walk

Very frequent (80-99%)HP:0002064

Spasticity of lower limb

Very frequent (80-99%)HP:0002061

Hand muscle weakness

Frequent (30-79%)HP:0030237

Lower limb amyotrophy

Frequent (30-79%)HP:0007210

Proximal neurogenic muscle weakness

Frequent (30-79%)HP:0003701

Spinal cord lesion

Frequent (30-79%)HP:0100561

Urgency frequency syndrome

Frequent (30-79%)HP:0000012

Increased reflexes

HP:0001347

Lower limb muscle weakness

HP:0007340

Spastic paraplegia

HP:0001258

Related Conditions

Pure hereditary spastic paraplegia(parent)

Autosomal dominant hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 763069002
UMLS CUI: C3888208
Fully Specified Name: Autosomal dominant spastic paraplegia type 41 (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.