ovalocytosis, hereditary hemolytic, with defective erythropoiesis

Preferred Label : ovalocytosis, hereditary hemolytic, with defective erythropoiesis;

Origin ID

C563479;

UMLS CUI

C1833689;

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