ALS9 - amyotrophic lateral sclerosis type 9

disorder

SNOMED 1204351003CUI C2678468

Overview

ALS9 - amyotrophic lateral sclerosis type 9 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.

Amyotrophic lateral sclerosis

HP:0007354

Distal muscle atrophy, upper and lower limbs

HP:0003693

Involuntary muscle stiffness, contraction, or spasm

HP:0001257

Weakness of outermost muscles

HP:0002460

Related Conditions

Autosomal dominant hereditary disorder(parent)

Chronic nervous system disease(parent)

Degenerative disorder(parent)

Hereditary disorder of nervous system(parent)

Amyotrophic lateral sclerosis(parent)

Quick Facts

SNOMED CT: 1204351003
UMLS CUI: C2678468
Fully Specified Name: Amyotrophic lateral sclerosis type 9 (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.