Autosomal recessive spastic paraplegia type 25

disorder

SNOMED 732933009CUI C2936860

Overview

Autosomal recessive spastic paraplegia type 25 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.

Herniated disk

Very frequent (80-99%)HP:0008441

Partial paralysis of legs

Very frequent (80-99%)HP:0002385

Lower limb pain

Frequent (30-79%)HP:0012514

Neck pain

Frequent (30-79%)HP:0030833

Sensory neuropathy

Frequent (30-79%)HP:0000763

Spastic paraplegia

Frequent (30-79%)HP:0001258

Abnormal lumbar spine morphology

Occasional (5-29%)HP:0100712

Abnormal peripheral nerve transmission

Occasional (5-29%)HP:0003134

Cataract, congenital

Occasional (5-29%)HP:0000519

Cervical spondylosis

Occasional (5-29%)HP:0008480

Infantile glaucoma

Occasional (5-29%)HP:0001087

Nerve damage causing decreased feeling and movement

Occasional (5-29%)HP:0007141

Upper limb pain

Occasional (5-29%)HP:0012513

Back pain

HP:0003418

Spinal cord compression

HP:0002176

Related Conditions

Complicated hereditary spastic paraplegia(parent)

Autosomal recessive hereditary spastic paraplegia(parent)

Quick Facts

SNOMED CT: 732933009
UMLS CUI: C2936860
Fully Specified Name: Autosomal recessive spastic paraplegia type 25 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.