myoglobinuria, recurrent

Preferred Label : myoglobinuria, recurrent;

Origin ID

C564018;

UMLS CUI

C1838877;

Currated CISMeF NLP mapping
- Genetic recurrent myoglobinuria [ICD-11 More detail]
- Genetic recurrent myoglobinuria [ORDO Disease]
- Genetic recurrent myoglobinuria (disorder) [SNOMED CT concept]
- Myoglobinuria, recurrent [OMIM Phenotype]
- Recurrent myoglobinuria [HPO term]
HPO term
- Recurrent myoglobinuria [HPO term]
MeSH term(s) associated for indexing
- myoglobinuria [MeSH Descriptor]
Record concept(s)
- myoglobinuria, recurrent [MeSH concept]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Genetic recurrent myoglobinuria [ORDO Disease]
- Myoglobinuria, recurrent [OMIM Phenotype]
- Recurrent myoglobinuria [HPO term]