Myosclerosis

disorder

SNOMED 763895001CUI C1850671

Overview

Myosclerosis 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.

Achilles tendon contracture

Always present (100%)HP:0001771

Elevated serum creatine phosphokinase

Always present (100%)HP:0003236

Decreased body height

Frequent (30-79%)HP:0004322

Facial muscle weakness of muscles innervated by CN VII

Frequent (30-79%)HP:0010628

Increased lumbar lordosis

HP:0002938

Muscle wasting

HP:0003202

Neck joint contracture

HP:0005997

Proximal limb muscle weakness

HP:0003701

Reduced forced vital capacity

HP:0032341

Spinal rigidity

HP:0003306

Thoracolumbar scoliosis

HP:0002944

Weakness of outermost muscles

HP:0002460

Related Conditions

Congenital disease(parent)

Disease of skeletal muscle(parent)

Recessive hereditary disorder (autosomal)(parent)

Hereditary disorder of musculoskeletal system(parent)

Hereditary disorder of nervous system(parent)

Quick Facts

SNOMED CT: 763895001
UMLS CUI: C1850671
Fully Specified Name: Myosclerosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.