Overview
Autosomal dominant myoglobinuria is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Acute kidney failure
HP:0001919
Elevated circulating creatine phosphokinase
HP:0003236
Muscle pain
HP:0003326
Muscle weakness
HP:0001324
Myoglobinuria
HP:0002913
Quick Facts
- SNOMED CT
- 725903003
- UMLS CUI
- C1834567
- Fully Specified Name
- Autosomal dominant myoglobinuria (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 5
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.