fanconi anemia, complementation group N

Preferred Label : fanconi anemia, complementation group N;

MeSH note : mutation in PALB2;

Origin ID

C563657;

UMLS CUI

C1835817;

Automatic exact mappings (from CISMeF team)
- FA complementation group C [ORDO Gene]
- FA complementation group L [ORDO Gene]
- Fanconi Anemia Complementation Group Protein [NCIt concept]
- Fanconi Anemia, Complementation Group C [NCIt concept]
- Fanconi Anemia, Complementation Group J [NCIt concept]
- Fanconi anemia, Complementation group C [OMIM Phenotype]
- Fanconi anemia, complementation group L [OMIM Phenotype]
- Fanconi anemia, complementation group j [OMIM Phenotype]
- Fanconi anemia, complementation group t [OMIM Phenotype]
- partner and localizer of BRCA2 [ORDO Gene]
Currated CISMeF NLP mapping
- Fanconi Anemia, Complementation Group N [NCIt concept]
- Fanconi anemia complementation group N [DO Concept]
- Fanconi anemia, complementation group n [OMIM Phenotype]
MeSH term(s) associated for indexing
- fanconi anemia [MeSH Descriptor]
Record concept(s)
- fanconi anemia, complementation group N [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fanconi Anemia, Complementation Group N [NCIt concept]
- Fanconi anemia complementation group N [DO Concept]
- Fanconi anemia, complementation group n [OMIM Phenotype]