Juvenile amyotrophic lateral sclerosis

disorder

SNOMED 718555006CUI C3468114

Overview

Juvenile amyotrophic lateral sclerosis 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

Very frequent (80-99%)HP:0007354

Distal muscle atrophy, upper and lower limbs

Very frequent (80-99%)HP:0003693

Muscle atrophy, neurogenic

Very frequent (80-99%)HP:0003202

Muscle weakness

Very frequent (80-99%)HP:0001324

Spasticity of lower limb

Very frequent (80-99%)HP:0002061

Upper extremity spasticity

Very frequent (80-99%)HP:0006986

Abnormal vocalization

Frequent (30-79%)HP:0002167

Arm dystonia

Frequent (30-79%)HP:0031960

Brisk deep tendon reflexes

Frequent (30-79%)HP:0001348

Bulbar signs

Frequent (30-79%)HP:0002483

CNS hypomyelination

Frequent (30-79%)HP:0003429

Contractures of the joints of the lower limbs

Frequent (30-79%)HP:0005750

Contractures of the joints of the upper limbs

Frequent (30-79%)HP:0100360

Delayed ability to walk

Frequent (30-79%)HP:0031936

Dystonic movements

Frequent (30-79%)HP:0001332

Gait disturbance

Frequent (30-79%)HP:0001288

Hypertonia

Frequent (30-79%)HP:0001276

Inability to walk

Frequent (30-79%)HP:0002540

Muscle fiber atrophy

Frequent (30-79%)HP:0100295

Spastic diparesis

Frequent (30-79%)HP:0001264

Weakness of outermost muscles

Frequent (30-79%)HP:0002460

Arc de cercle

Occasional (5-29%)HP:0002179

Ataxia

Occasional (5-29%)HP:0001251

Axial dystonia

Occasional (5-29%)HP:0002530

Behavioral symptoms

Occasional (5-29%)HP:0000708

Cachexia

Occasional (5-29%)HP:0004326

Cerebellar abnormality

Occasional (5-29%)HP:0001317

Choreiform movements

Occasional (5-29%)HP:0002072

Clonus

Occasional (5-29%)HP:0002169

Cognitive deficits

Occasional (5-29%)HP:0100543

Related Conditions

Juvenile amyotrophic lateral sclerosis type 2(child)

ALS5 - amyotrophic lateral sclerosis type 5(child)

Amyotrophic lateral sclerosis(parent)

Hereditary disorder of nervous system(parent)

Chronic nervous system disease(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 718555006
UMLS CUI: C3468114
Fully Specified Name: Juvenile amyotrophic lateral sclerosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.