fanconi anemia, complementation group I

Preferred Label : fanconi anemia, complementation group I;

MeSH note : mutation in FANCI;

Origin ID

C563802;

UMLS CUI

C1836861;

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