ovalocytosis, Malaysian-Melanesian-Filipino type

Preferred Label : ovalocytosis, Malaysian-Melanesian-Filipino type;

Origin ID

C566230;

UMLS CUI

C1862322;

Currated CISMeF NLP mapping
- Ovalocytosis, southeast asian [OMIM Phenotype]
- Southeast Asian ovalocytosis [ORDO Disease]
- Southeast Asian ovalocytosis [ICD-11 More detail]
- Southeast Asian ovalocytosis (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- elliptocytosis, hereditary [MeSH Descriptor]
Record concept(s)
- ovalocytosis, Malaysian-Melanesian-Filipino type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ovalocytosis, southeast asian [OMIM Phenotype]
- Southeast Asian ovalocytosis (disorder) [SNOMED CT concept]