myoglobinuria, acute recurrent, autosomal recessive

Preferred Label : myoglobinuria, acute recurrent, autosomal recessive;

MeSH synonym : myoglobinuria, familial paroxysmal paralytic; rhabdomyolysis, acute recurrent;

Détails

Origin ID

C564832;

UMLS CUI

C1849386;

Currated CISMeF NLP mapping
- Myoglobinuria, acute recurrent, autosomal recessive [OMIM Phenotype]
MeSH term(s) associated for indexing
- myoglobinuria [MeSH Descriptor]
Record concept(s)
- myoglobinuria, acute recurrent, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myoglobinuria, acute recurrent, autosomal recessive [OMIM Phenotype]

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

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