Amyotrophic lateral sclerosis type 3

disorder

SNOMED 1201950008CUI C1847735

Overview

Amyotrophic lateral sclerosis type 3 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.

Bulbar signs

Always present (100%)HP:0002483

Lower limb muscle weakness

Always present (100%)HP:0007340

Infratentorial atrophy

Excluded (<1%)HP:0001272

Progressive dementia

Excluded (<1%)HP:0000726

Related Conditions

Autosomal dominant hereditary disorder(parent)

Chronic nervous system disease(parent)

Hereditary disorder of nervous system(parent)

Amyotrophic lateral sclerosis(parent)

Degenerative disorder(parent)

Quick Facts

SNOMED CT: 1201950008
UMLS CUI: C1847735
Fully Specified Name: Amyotrophic lateral sclerosis type 3 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 4

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.