lymphoblastic transformation, intrinsic defect in

Preferred Label : lymphoblastic transformation, intrinsic defect in;

Is substance : O;

Origin ID

C565431;

UMLS CUI

C1855474;

Currated CISMeF NLP mapping
- Lymphoblastic transformation, intrinsic defect in [OMIM Phenotype]
MeSH term(s) associated for indexing
- immunologic deficiency syndromes [MeSH Descriptor]
Record concept(s)
- lymphoblastic transformation, intrinsic defect in [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lymphoblastic transformation, intrinsic defect in [OMIM Phenotype]