congenital anemia inherited aplastic anemia developmental anomaly of metabolic origin polymalformative genetic syndrome with increased risk of developing cancer syndrome with limb reduction defects dysostosis of genetic origin with limb anomaly as a major feature inborn errors of metabolism hyperpigmentation of the skin Fanconi anemia DOID:13636 Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. Fanconi pancytopenia Fanconi panmyelopathy Fanconi's anemia GARD:0006425 ICD10:D61.0 ICD10:D61.09 ICD9:284.09 MESH:D005199 MONDO:0019391 MedDRA:10055206 NCIT:C62505 OMIMPS:227650 Orphanet:84 Panmyelopathy, Fanconi SCTID:30575002 UMLS:C0015625 pancytopenia, congenital primary erythroid hypoplasia hematological disorder with renal involvement DNA repair disease genetic skin disease genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability