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Fanconi anemia complementation group O | RareConnect | RareConnect.io

/Fanconi anemia

/Fanconi anemia complementation group O

Fanconi anemia complementation group O

Rare Disease

MONDO:0013248

Also Known As

FANCOFanconi Anemia, complementation group type OFanconi anaemia caused by mutation in RAD51CFanconi anaemia caused by mutation in Rad51CFanconi anaemia complementation group type OFanconi anemia caused by mutation in RAD51CFanconi anemia caused by mutation in Rad51CFanconi anemia complementation group type ORAD51C Fanconi anaemiaRAD51C Fanconi anemiaRad51C Fanconi anaemiaRad51C Fanconi anemiaFanconi anemia, complementation group O

Definition

Any Fanconi anemia in which the cause of the disease is a mutation in the RAD51C 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:613390 ↗

GARD

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