Fanconi anemia complementation group L

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Disease Overview

Any Fanconi anemia in which the cause of the disease is a mutation in the FANCL gene.

Synonyms

FANCL
FANCL Fanconi anaemia
FANCL Fanconi anemia
Fanconi Anemia, complementation Group 50
Fanconi Anemia, complementation group type 50
Fanconi anaemia caused by mutation in FANCL
Fanconi anaemia complementation group type L
Fanconi anemia caused by mutation in FANCL
Fanconi anemia complementation group L
Fanconi anemia complementation group type L
Fanconi anemia, complementation group L

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.