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.

Autosomal recessive spastic paraplegia type 24 — Symptoms, Testing & Specialists | Ltrl