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Fanconi anemia complementation group T | RareConnect | RareConnect.io

/Fanconi anemia

/Fanconi anemia complementation group T

Fanconi anemia complementation group T

Rare Disease

MONDO:0014638

Also Known As

FANCTFanconi Anemia, complementation group type TFanconi anaemia caused by mutation in UBE2TFanconi anaemia complementation group type TFanconi anemia caused by mutation in UBE2TFanconi anemia complementation group type TUBE2T Fanconi anaemiaUBE2T Fanconi anemiaFanconi anemia, complementation group T

Definition

Any Fanconi anemia in which the cause of the disease is a mutation in the UBE2T 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:616435 ↗

GARD

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