elliptocytosis 1

Preferred Label : elliptocytosis 1;

MeSH note : PROM mutation in EPB41;

MeSH synonym : elliptocytosis, Rhesus-Linked type; protein 4.1 of erythrocyte membrane, defect of; 4.1-Minus trait;

Details

Origin ID

C567520;

UMLS CUI

C2678497;

Currated CISMeF NLP mapping
- Elliptocytosis 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- elliptocytosis, hereditary [MeSH Descriptor]
Record concept(s)
- elliptocytosis 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Elliptocytosis 1 [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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