Autosomal recessive spastic paraplegia type 24

disorder

SNOMED 785304005CUI C1843569

Overview

Autosomal recessive spastic paraplegia type 24 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.

Clonus

Very frequent (80-99%)HP:0002169

Increased reflexes

Very frequent (80-99%)HP:0001347

Involuntary muscle stiffness, contraction, or spasm

Very frequent (80-99%)HP:0001257

Scissor gait

Very frequent (80-99%)HP:0012407

Walking on tiptoes

Very frequent (80-99%)HP:0030051

Sensorineural deafness

Frequent (30-79%)HP:0000407

Spastic paraplegia

HP:0001258

Standing instability

HP:0003698

Related Conditions

Pure hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 785304005
UMLS CUI: C1843569
Fully Specified Name: Autosomal recessive spastic paraplegia type 24 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.