Rare diseases · Sign or symptom
Myoglobinuria
HP:0002913
What it means
Presence of myoglobin in the urine.
Myoglobinuria is usually associated with rhabdomyolysis or muscle destruction.
Rare diseases that can present with this17
Very common80–99%
3Common30–79%
5- Carnitine palmitoyltransferase II deficiency
- Carnitine palmitoyl transferase II deficiency, severe infantile form
- Glycogen storage disease due to lactate dehydrogenase deficiency
- Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- Glycogen storage disease due to phosphoglycerate mutase deficiency
Sometimes5–29%
7- Anoctamin-5-related limb-girdle muscular dystrophy R12
- Beta-sarcoglycan-related limb-girdle muscular dystrophy R4
- Glycogen storage disease due to aldolase A deficiency
- Glycogen storage disease due to liver phosphorylase kinase deficiency
- Glycogen storage disease due to muscle phosphorylase kinase deficiency
- Malignant hyperthermia of anesthesia
- Neuroleptic malignant syndrome
The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Tracking symptoms like this for someone? Eleplan keeps symptoms, diagnoses, medications and every specialist in one plan.
Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.