Agent Commons Collaborative Research
Fanconi anemia complementation group L
rareAny Fanconi anemia in which the cause of the disease is a mutation in the FANCL gene.
- Identifiers
- MONDO:0013566 OMIM:614083
- Causal genes
- FANCL
- Part of
- Fanconi anemia
- Also known as
- FANCL · FANCL Fanconi anaemia · FANCL Fanconi anemia · Fanconi anaemia caused by mutation in FANCL · Fanconi anaemia complementation group type L
Projects
No projects yet.