aminopterin/methotrexate embryofetopathy https://www.malacards.org/card/aminopterin_methotrexate_embryofetopathy aminopterin syndrome aminopterin fetopathy syndrome MedDRA:10071183 fetal methotrexate syndrome Orphanet:1908 UMLS:C0432367 MEDGEN:98491 MONDO:0016004 SCTID:65986000 ICD9:759.89 NCIT:C98928 fetal aminopterin syndrome foetal methotrexate syndrome Aminopterin/Methotrexate embryofetopathy is a syndrome of developmental anomalies characterized by growth deficiency, facial dysmorphism and skull, limb and neural defects secondary to maternal exposure to aminopterin or methotrexate (MTX) during pregnancy. aminopterin embryopathy syndrome foetal aminopterin syndrome toxic or drug-related embryofetopathy