Autosomal recessive spastic paraplegia type 28

disorder

SNOMED 763376002CUI C1836295

Overview

Autosomal recessive spastic paraplegia type 28 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.

Extensor plantar responses

Very frequent (80-99%)HP:0003487

Increased reflexes

Very frequent (80-99%)HP:0001347

Abolished vibration sense

Frequent (30-79%)HP:0006944

Absence of pain sensation

Frequent (30-79%)HP:0007021

Axonal neuropathy

Frequent (30-79%)HP:0003477

Imbalance

Frequent (30-79%)HP:0002172

Loss of tactile sensation

Frequent (30-79%)HP:0010830

Lower limb muscle weakness

Frequent (30-79%)HP:0007340

Muscle rigidity

Frequent (30-79%)HP:0002063

Pes cavus

Frequent (30-79%)HP:0001761

Scoliosis

Frequent (30-79%)HP:0002650

Spastic paraplegia

Frequent (30-79%)HP:0001258

Spastic walk

Frequent (30-79%)HP:0002064

Spasticity of lower limb

Frequent (30-79%)HP:0002061

Unsteady walk

Frequent (30-79%)HP:0002317

Gait disturbance

HP:0001288

Loss of distal sensation

HP:0002936

Related Conditions

Pure hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 763376002
UMLS CUI: C1836295
Fully Specified Name: Autosomal recessive spastic paraplegia type 28 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 17

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.