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These terms define your current search. Click the × to remove a term. C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Nervous System Malformations [MESH:D009421] > Agenesis of Corpus Callosum [MESH:D061085] > Proud Syndrome [MESH:C563110] × 12 results Group by: C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities Sort by: MeSH_UID, MeSH_NAME   MESH:C006780   bisphenol A C006780               MESH:C009618   O,O-diethyl O-3,5,6-trichloro-2-pyridyl phosphate C009618               MESH:C012589   trichostatin A C012589               MESH:C029497   2,3-bis(3'-hydroxybenzyl)butyrolactone C029497               MESH:C563110   Proud Syndrome C563110               MESH:D000082   Acetaminophen D000082               MESH:D001104   Arbutin D001104               MESH:D003375   Coumestrol D003375               MESH:D003993   Dibutyl Phthalate D003993               MESH:D005839   Gentamicins D005839               MESH:D014635   Valproic Acid D014635               MESH:D019327   Copper Sulfate D019327