ALS5 - amyotrophic lateral sclerosis type 5

disorder

SNOMED 1201961000CUI C1865864

Overview

ALS5 - amyotrophic lateral sclerosis type 5 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.

Corticospinal signs

Always present (100%)HP:0007256

Distal limb muscle weakness due to peripheral neuropathy

Always present (100%)HP:0002460

Distal muscle atrophy, upper and lower limbs

Always present (100%)HP:0003693

Bulbar signs

Frequent (30-79%)HP:0002483

Muscle fasciculation

Frequent (30-79%)HP:0002380

Respiratory failure due to muscle weakness

Occasional (5-29%)HP:0002747

Urinary incontinence

Very rare (1-4%)HP:0000020

Abnormality of the cerebral white matter

Excluded (<1%)HP:0002500

Amyotrophic lateral sclerosis

HP:0007354

Cognitive deficits

Excluded (<1%)HP:0100543

Difficulty articulating speech

HP:0001260

Extensor plantar responses

HP:0003487

Increased reflexes

HP:0001347

Involuntary muscle stiffness, contraction, or spasm

HP:0001257

Lower motor neuron manifestations

HP:0002366

Thinning of the corpus callosum

Excluded (<1%)HP:0033725

Related Conditions

Juvenile amyotrophic lateral sclerosis(parent)

Quick Facts

SNOMED CT: 1201961000
UMLS CUI: C1865864
Fully Specified Name: Juvenile amyotrophic lateral sclerosis type 5 (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.