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Fanconi anemia complementation group V | RareConnect | RareConnect.io

/Fanconi anemia

/Fanconi anemia complementation group V

Fanconi anemia complementation group V

Rare Disease

MONDO:0014985

Also Known As

FANCVFanconi Anemia, complementation group VFanconi Anemia, complementation group type VFanconi anaemia caused by mutation in MAD2L2Fanconi anaemia complementation group type VFanconi anemia caused by mutation in MAD2L2Fanconi anemia complementation group type VMAD2L2 Fanconi anaemiaMAD2L2 Fanconi anemiaFanconi Anemia, complementation Group 5Fanconi anemia, complementation GROUP V

Definition

Any Fanconi anemia in which the cause of the disease is a mutation in the MAD2L2 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:617243 ↗

GARD

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