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Fanconi anemia complementation group B | RareConnect | RareConnect.io

/Fanconi anemia

/Fanconi anemia complementation group B

Fanconi anemia complementation group B

Rare Disease

MONDO:0010351

Also Known As

FA2FACBFANCBFanconi Anemia, complementation group type BFanconi anaemia complementation group type BFanconi anemia complementation group BFanconi anemia complementation group type BFanconi anemia, complementation group B, X-linked recessiveFanconi pancytopenia type 2Fanconi anemia, complementation group BFanconi pancytopenia, type 2

Definition

Fanconi anemia caused by mutations of the FANCB gene. This gene encodes the protein for complementation group B.

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:300514 ↗

GARD

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