congenital anemia inherited aplastic anemia bone marrow disorder multiple congenital anomalies/dysmorphic syndrome without intellectual disability developmental anomaly of metabolic origin dysostosis hyperpigmentation of the skin Fanconi anemia https://github.com/monarch-initiative/mondo/issues/5682 NANDO:2200652 NANDO:1200303 NORD:1132 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. GARD:0006425 DOID:13636 UMLS:C0015625 MONDO:0019391 SCTID:30575002 Fanconi anemia Fanconi pancytopenia MEDGEN:41967 Fanconi's anemia ICD9:284.09 OMIMPS:227650 primary erythroid hypoplasia MESH:D005199 pancytopenia, congenital MedDRA:10055206 NCIT:C62505 NANDO:1200891 Orphanet:84 Panmyelopathy, Fanconi DNA repair disease telomere syndrome