leukocyte nuclear appendages, hereditary prevalence of

Preferred Label : leukocyte nuclear appendages, hereditary prevalence of;

Origin ID

C563626;

UMLS CUI

C1835405;

Currated CISMeF NLP mapping
- Leukocyte nuclear appendages, hereditary prevalence of [OMIM Phenotype]
MeSH term(s) associated for indexing
- leukocyte disorders [MeSH Descriptor]
Record concept(s)
- leukocyte nuclear appendages, hereditary prevalence of [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Leukocyte nuclear appendages, hereditary prevalence of [OMIM Phenotype]