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Disease Ontology Browser
Fanconi anemia complementation group C (DOID:0111087)
Alliance: disease page
Synonyms: FA3; FACC; FANCC; Fanconi pancytopenia type 3
Alt IDs: OMIM:227645
Definition: A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/18/2020
MGI 6.14
The Jackson Laboratory