Autosomal dominant myoglobinuria

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.;

Détails

Origin ID

149859272;

UMLS CUI

C1834567;

Currated CISMeF NLP mapping
- Autosomal dominant myoglobinuria [ORDO Disease]
- Autosomal dominant myoglobinuria (disorder) [SNOMED CT concept]
- Myoglobinuria, autosomal dominant [OMIM Phenotype]
- myoglobinuria, autosomal dominant [MeSH Supplementary Concept]
- myoglobinuria, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant myoglobinuria [ORDO Disease]
- Autosomal dominant myoglobinuria (disorder) [SNOMED CT concept]
- Myoglobinuria, autosomal dominant [OMIM Phenotype]
- myoglobinuria, autosomal dominant [MeSH concept]
- myoglobinuria, autosomal dominant [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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