Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Neuroleptic malignant syndrome
Occasional (5-29%)
Glycogen storage disease, type V
Frequent (30-79%)
Muscle phosphoglycerate mutase deficiency
Deficiency of beta-keto-reductase
Malignant hyperthermia caused by anesthesia
Occasional (5-29%)
Glycogen phosphorylase kinase deficiency
Occasional (5-29%)
Mitochondrial trifunctional protein deficiency
CPTII - Carnitine palmitoyltransferase deficiency type II
Frequent (30-79%)
Becker muscular dystrophy
Very frequent (80-99%)
Malignant hyperthermia
Myopathy with deficiency of succinate dehydrogenase and aconitase
Autosomal recessive limb girdle muscular dystrophy type 2E
Occasional (5-29%)
Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Very rare (1-4%)
Autosomal dominant myoglobinuria
Autosomal recessive limb girdle muscular dystrophy type 2L
Occasional (5-29%)
Maternal uniparental disomy of chromosome 21
Frequent (30-79%)
Glycogen storage disease due to muscle phosphorylase kinase deficiency
Occasional (5-29%)
Glycogen storage disease due to liver and muscle glycogen phosphorylase kinase deficiency
Very rare (1-4%)
Transport and golgi organization 2 homolog-related metabolic encephalopathy, arrhythmia syndrome
Always present (100%)
Glycogen storage disease type XI
Frequent (30-79%)
Glycogen storage disease due to aldolase A deficiency
Occasional (5-29%)
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
Frequent (30-79%)
Myopathic form of carnitine palmitoyltransferase II deficiency
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 48165008
- UMLS CUI
- C0027080
- Fully Specified Name
- Myoglobinuria (finding)
- Associated Conditions
- 23
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.