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Fanconi anemia complementation group U | RareConnect | RareConnect.io

/Fanconi anemia

/Fanconi anemia complementation group U

Fanconi anemia complementation group U

Rare Disease

MONDO:0014987

Also Known As

FANCUFanconi Anemia, complementation group UFanconi Anemia, complementation group type UFanconi anaemia caused by mutation in XRCC2Fanconi anaemia complementation group type UFanconi anemia caused by mutation in XRCC2Fanconi anemia complementation group type UXRCC2 Fanconi anaemiaXRCC2 Fanconi anemiaFanconi anemia, complementation GROUP U

Definition

Any Fanconi anemia in which the cause of the disease is a mutation in the XRCC2 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:617247 ↗

GARD

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