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Glycogen heart disease

disorder
SNOMED 274864009CUI C0017921

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.

Difficulty descending stairs
Always present (100%)HP:0033235
Electrical right axis deviation
Always present (100%)HP:0033567
Fluid around lungs
Always present (100%)HP:0002202
Increased circulating creatine kinase MB isoform
Always present (100%)HP:0032232
Increased circulating NT-proBNP concentration
Always present (100%)HP:0031185
Increased muscle glycogen content
Always present (100%)HP:0009051
Limb muscle weakness
Always present (100%)HP:0003690
Nonimmune hydrops fetalis
Always present (100%)HP:0001790
Panting
Always present (100%)HP:0002094
Sinus tach
Always present (100%)HP:0011703
Subarachnoid hemorrhage
Always present (100%)HP:0002138
Urinary incontinence
Always present (100%)HP:0000020
Decreased circulating acid maltase activity
Very frequent (80-99%)HP:0034932
Muscle weakness
Very frequent (80-99%)HP:0001324
Muscle weakness, progressive, proximal
Very frequent (80-99%)HP:0009073
Oligosacchariduria
Very frequent (80-99%)HP:0010471
Alanine aminotransferase increased
Frequent (30-79%)HP:0031964
Areflexia
Frequent (30-79%)HP:0001284
Camptocormia
Frequent (30-79%)HP:0100595
Cardiac murmur
Frequent (30-79%)HP:0030148
Decreased facial muscle movement
Frequent (30-79%)HP:0000338
Difficulty walking up stairs
Frequent (30-79%)HP:0003551
Elevated serum creatine phosphokinase
Frequent (30-79%)HP:0003236
EMG: myopathic changes
Frequent (30-79%)HP:0003458
Enlarged liver
Frequent (30-79%)HP:0002240
Exertional dyspnea
Frequent (30-79%)HP:0002875
Feeding difficulties in infancy
Frequent (30-79%)HP:0008872
Gait disturbance
Frequent (30-79%)HP:0001288
Glycogen accumulation in muscle fibre lysosomes
Frequent (30-79%)HP:0030231
Growth deficiency
Frequent (30-79%)HP:0001510

Quick Facts

SNOMED CT
274864009
UMLS CUI
C0017921
Fully Specified Name
Glycogen storage disease due to acid maltase deficiency (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
Known Treatments
3
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.