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Fanconi anemia complementation group L | RareConnect | RareConnect.io

/Fanconi anemia

/Fanconi anemia complementation group L

Fanconi anemia complementation group L

Rare Disease

MONDO:0013566

Also Known As

FANCLFANCL Fanconi anaemiaFANCL Fanconi anemiaFanconi Anemia, complementation group type 50Fanconi anaemia caused by mutation in FANCLFanconi anaemia complementation group type LFanconi anemia caused by mutation in FANCLFanconi anemia complementation group LFanconi anemia complementation group type LFanconi Anemia, complementation Group 50Fanconi anemia, complementation group L

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614083 ↗

GARD

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Fanconi anemia complementation group E

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Fanconi anemia complementation group F

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