Fanconi anemia complementation group L

MONDO:0013566

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

Also known as: FANCL, FANCL Fanconi anaemia, FANCL Fanconi anemia, 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

12 clinical trials for this condition and its sub-types, 0 tagged with Fanconi anemia complementation group L itself.

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↑ Fanconi anemia (42)

Including sub-types (12) Tagged with Fanconi anemia complementation group L (0)

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