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Disease Ontology Browser
Fanconi anemia (DOID:13636)
Alliance: disease page
Synonyms: Fanconi anaemia; Fanconi pancytopenia; Fanconi panmyelopathy; Fanconi's anaemia; Fanconi's anemia
Alt IDs: ICD10CM:D61.09, MESH:D005199, NCI:C62505, OMIM:PS227650, ORDO:84, UMLS_CUI:C0015625
Definition: A congenital hypoplastic anemia characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. It is a result of a genetic defect in a cluster of proteins responsible for DNA repair.

Disease References using Mouse Models (14)

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
04/16/2024
MGI 6.23
The Jackson Laboratory