Myoglobinuriacauses

Causes by Organ System

Cardiovascular	Myocardial infarction, Myocarditis
Chemical/Poisoning	Haff disease, Snake bite , Venom
Dental	No underlying causes
Dermatologic	Dermatomyositis
Drug Side Effect	Barbiturates, Carbenoxolone, Diamorphine, Fibrate, Malignant hyperpyrexia, Neuroleptic malignant syndrome, Statins, Trabectedin
Ear Nose Throat	No underlying causes
Endocrine	No underlying causes
Environmental	Heat stroke
Gastroenterologic	No underlying causes
Genetic	Brody myopathy, Carnitine palmitoyltransferase 1 deficiency, Carnitine palmitoyltransferase 2 deficiency, Familial paroxysmal rhabdomyolysis, Glycogen storage disease type V, Myopathy with deficiency of succinate dehydrogenase and aconitase, Phosphoglycerate kinase deficiency, Phosphogylcerate mutase 2 deficiency, Very long-chain acyl-coenzyme A dehydrogenase deficiency
Hematologic	No underlying causes
Iatrogenic	No underlying causes
Infectious Disease	No underlying causes
Musculoskeletal/Orthopedic	Brody myopathy, Compartment syndrome, Dermatomyositis, Polymyositis, Rhabdomyolysis
Neurologic	Choreoathetosis, Seizures
Nutritional/Metabolic	No underlying causes
Obstetric/Gynecologic	No underlying causes
Oncologic	No underlying causes]
Ophthalmologic	No underlying causes
Overdose/Toxicity	No underlying causes
Psychiatric	No underlying causes
Pulmonary	No underlying causes
Renal/Electrolyte	Hypokalaemia, Hypophosphataemia
Rheumatology/Immunology/Allergy	Dermatomyositis, Polymyositis
Sexual	No underlying causes
Trauma	Burns, Crush syndrome, Electric shock, Trauma
Urologic	No underlying causes
Miscellaneous	Exercise, Meyer-betz disease

Causes in Alphabetical Order

• Barbiturates
• Brody myopathy
• Burns
• Carbenoxolone
• Carnitine palmitoyltransferase 1 deficiency
• Carnitine palmitoyltransferase 2 deficiency
• Choreoathetosis
• Compartment syndrome
• Crush syndrome
• Dermatomyositis
• Diamorphine
• Electric shock
• Exercise
• Familial paroxysmal rhabdomyolysis
• Fibrate
• Glycogen storage disease type V
• Haff disease
• Heat stroke
• Hypokalaemia
• Hypophosphataemia
• Malignant hyperpyrexia
• Meyer-Betz disease
• Myocardial infarction
• Myocarditis
• Myopathy with deficiency of succinate dehydrogenase and aconitase
• Neuroleptic malignant syndrome
• Phosphoglycerate kinase deficiency
• Phosphoglycerate mutase deficiency
• Polymyositis
• Rhabdomyolysis
• Seizures
• Snake bite
• Statins
• Trabectedin
• Trauma
• Venom
• Very long-chain acyl-coenzyme A dehydrogenase deficiency