Preferred Label : Autosomal dominant myoglobinuria;
ICD-11 definition : This refers to an autosomal dominant presence of myoglobin in the urine, usually associated
with rhabdomyolysis or muscle destruction.;
Origin ID : 149859272;
UMLS CUI : C1834567;
Currated CISMeF NLP mapping
Semantic type(s)
UMLS correspondences (same concept)
This refers to an autosomal dominant presence of myoglobin in the urine, usually associated
with rhabdomyolysis or muscle destruction.