ALS10 - amyotrophic lateral sclerosis type 10

disorder

SNOMED 1208412003CUI C2677565

Overview

ALS10 - amyotrophic lateral sclerosis type 10 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

Always present (100%)HP:0007354

Deglutition disorder

HP:0002015

Difficulty articulating speech

HP:0001260

Emotional lability

HP:0000712

Extensor plantar responses

HP:0003487

Frontotemporal dementia

HP:0002145

Impulse control disorders

HP:0000734

Involuntary muscle stiffness, contraction, or spasm

HP:0001257

Lack of feeling, emotion, interest

HP:0000741

Muscle weakness

HP:0001324

Neurogenic muscle atrophy, especially in the lower limbs

HP:0003202

Perseverative behaviour

HP:0030223

Respiratory failure due to muscle weakness

HP:0002747

Stimming

HP:0000733

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: 1208412003
UMLS CUI: C2677565
Fully Specified Name: Amyotrophic lateral sclerosis type 10 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.