CD59 deficiency

Preferred Label : CD59 deficiency;

MeSH note : mutation in CD59;

Origin ID

C567355;

UMLS CUI

C2676767;

Automatic exact mappings (from CISMeF team)
- CD59.deficient [LOINC component]
Currated CISMeF NLP mapping
- Hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy [OMIM Phenotype]
- Primary CD59 deficiency [ORDO Disease]
- Primary CD59 deficiency (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- anemia, hemolytic [MeSH Descriptor]
- hemoglobinuria [MeSH Descriptor]
Record concept(s)
- CD59 deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy [OMIM Phenotype]
- Primary CD59 deficiency [ORDO Disease]