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Disease Ontology Browser
Fanconi anemia (DOID:13636)
Synonyms: Fanconi pancytopenia; Fanconi panmyelopathy; Fanconi's anemia
Alt IDs: OMIM:227645, OMIM:227646, OMIM:227650, OMIM:300514, OMIM:600901, OMIM:603467, OMIM:605724, OMIM:609053, OMIM:609054, OMIM:610832, OMIM:613390, OMIM:613951, OMIM:614082, OMIM:614083, OMIM:615272, OMIM:616435, OMIM:617243, OMIM:617244, OMIM:617247, ICD10CM:D61.09, MESH:D005199, NCI:C62505, 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 (13)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/18/2017
MGI 6.08
The Jackson Laboratory