elliptocytosis, atypical

Preferred Label : elliptocytosis, atypical;

Origin ID

C565598;

UMLS CUI

C1857010;

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