fanconi anemia, complementation group B

Preferred Label : fanconi anemia, complementation group B;

MeSH note : mutation in FANCB;

MeSH synonym : fanconi pancytopenia, type 2;

Origin ID

C564497;

UMLS CUI

C1845292;

Currated CISMeF NLP mapping
- Fanconi Anemia, Complementation Group B [NCIt concept]
- Fanconi anemia complementation group B [DO Concept]
- Fanconi anemia, complementation group b [OMIM Phenotype]
MeSH term(s) associated for indexing
- fanconi anemia [MeSH Descriptor]
Record concept(s)
- fanconi anemia, complementation group B [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fanconi Anemia, Complementation Group B [NCIt concept]
- Fanconi anemia complementation group B [DO Concept]
- Fanconi anemia, complementation group b [OMIM Phenotype]