Autosomal dominant spastic paraplegia type 13

disorder

SNOMED 783698005CUI C1854467

Overview

Autosomal dominant spastic paraplegia type 13 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

Sphincter disturbances

Very frequent (80-99%)HP:0002839

Corticospinal signs

Frequent (30-79%)HP:0007256

Distal sensory loss, especially vibratory sense

Frequent (30-79%)HP:0002166

Extensor plantar responses

Frequent (30-79%)HP:0003487

Increased reflexes

Frequent (30-79%)HP:0001347

Lower limb muscle weakness

Frequent (30-79%)HP:0007340

Spastic walk

Frequent (30-79%)HP:0002064

Spasticity of lower limb

Frequent (30-79%)HP:0002061

Upper limb hyperreflexia

Frequent (30-79%)HP:0007350

Urinary incontinence

Frequent (30-79%)HP:0000020

Pes cavus

Occasional (5-29%)HP:0001761

Scoliosis

Occasional (5-29%)HP:0002650

Urinary urgency

Occasional (5-29%)HP:0000012

Hearing impairment

Very rare (1-4%)HP:0000365

Rod-cone dystrophy

Very rare (1-4%)HP:0000510

Related Conditions

Autosomal dominant hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 783698005
UMLS CUI: C1854467
Fully Specified Name: Autosomal dominant spastic paraplegia type 13 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.