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Fanconi anemia complementation group P | RareConnect | RareConnect.io

/Fanconi anemia

/Fanconi anemia complementation group P

Fanconi anemia complementation group P

Rare Disease

MONDO:0013499

Also Known As

FANCPFanconi Anemia, complementation group type PFanconi anaemia caused by mutation in SLX4Fanconi anaemia caused by mutation in Slx4Fanconi anaemia complementation group type PFanconi anemia caused by mutation in SLX4Fanconi anemia caused by mutation in Slx4Fanconi anemia complementation group type PSLX4 Fanconi anaemiaSLX4 Fanconi anemiaSlx4 Fanconi anaemiaSlx4 Fanconi anemiaFanconi anemia, complementation group P

Definition

Any Fanconi anemia in which the cause of the disease is a mutation in the SLX4 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:613951 ↗

GARD

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Fanconi anemia complementation group E

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Fanconi anemia complementation group F

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