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Becker muscular dystrophy

disorder
SNOMED 387732009CUI C0013264

Overview

Source: MedlinePlus.gov, National Library of Medicine. 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
Delayed gross motor development
Always present (100%)HP:0002194
Flexion contractures of knees
Always present (100%)HP:0006380
Hamstring contractures
Always present (100%)HP:0003089
Loss of ambulation
Always present (100%)HP:0002505
Obstructive sleep apnea
Always present (100%)HP:0002870
Respiratory failure due to muscle weakness
Always present (100%)HP:0002747
Restrictive respiratory disease
Always present (100%)HP:0002091
Abnormal urinary color
Very frequent (80-99%)HP:0012086
Cognitive deficits
Very frequent (80-99%)HP:0100543
Cognitive delay
Very frequent (80-99%)HP:0001263
Delayed motor milestones
Very frequent (80-99%)HP:0001270
Difficulty walking up stairs
Very frequent (80-99%)HP:0003551
Elevated serum creatine phosphokinase
Very frequent (80-99%)HP:0003236
Flexion contractures
Very frequent (80-99%)HP:0001371
Gait disturbance
Very frequent (80-99%)HP:0001288
Increased size of calf muscles
Very frequent (80-99%)HP:0008981
Muscle pain
Very frequent (80-99%)HP:0003326
Myoglobinuria
Very frequent (80-99%)HP:0002913
Poor exercise tolerance
Very frequent (80-99%)HP:0003546
Progressive muscle weakness
Very frequent (80-99%)HP:0003323
Proximal neurogenic muscle weakness
Very frequent (80-99%)HP:0003701
Respiratory insufficiency
Very frequent (80-99%)HP:0002093
Scoliosis
Very frequent (80-99%)HP:0002650
Specific learning disability
Very frequent (80-99%)HP:0001328
Speech and language difficulties
Very frequent (80-99%)HP:0000750
Waddling gait
Very frequent (80-99%)HP:0002515
Abnormality of the lower limb
Frequent (30-79%)HP:0002814
Falls
Frequent (30-79%)HP:0002527
Muscle spasm
Frequent (30-79%)HP:0003394

Quick Facts

SNOMED CT
387732009
UMLS CUI
C0013264
Fully Specified Name
Becker muscular dystrophy (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
Known Treatments
6
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.