DISEASES      Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]      Congenital, Hereditary, and Neonatal Diseases and Abnormalities           Congenital Abnormalities [C16.131] +           Congenital Abnormalities +                Abnormalities, Drug Induced [C16.131.042]                Abnormalities, Drug Induced                Abnormalities, Multiple [C16.131.077] +                Abnormalities, Multiple +                Abnormalities, Radiation Induced [C16.131.080]                Abnormalities, Radiation Induced                Abnormalities, Severe Teratoid [C16.131.085] +                Abnormalities, Severe Teratoid +                Aicardi Syndrome [C16.131.162]                Aicardi Syndrome                Cardiovascular Abnormalities [C16.131.240] +                Cardiovascular Abnormalities +                Chromosome Disorders [C16.131.260] +                Chromosome Disorders +                Congenital Microtia [C16.131.287]                Congenital Microtia                Digestive System Abnormalities [C16.131.314] +                Digestive System Abnormalities +                Eye Abnormalities [C16.131.384] +                Eye Abnormalities +                Hernias, Diaphragmatic, Congenital [C16.131.433]                Hernias, Diaphragmatic, Congenital                Lymphatic Abnormalities [C16.131.482] +                Lymphatic Abnormalities +                Musculoskeletal Abnormalities [C16.131.621] +                Musculoskeletal Abnormalities +                Nervous System Malformations [C16.131.666] +                Nervous System Malformations +                Respiratory System Abnormalities [C16.131.740] +                Respiratory System Abnormalities +                Situs Inversus [C16.131.810] +                Situs Inversus +                Skin Abnormalities [C16.131.831] +                Skin Abnormalities +                Stomatognathic System Abnormalities [C16.131.850] +                Stomatognathic System Abnormalities +                Thyroid Dysgenesis [C16.131.894] +                Thyroid Dysgenesis +                Urogenital Abnormalities [C16.131.939] +                Urogenital Abnormalities +           Fetal Diseases [C16.300] +           Fetal Diseases +           Genetic Diseases, Inborn [C16.320] +           Genetic Diseases, Inborn +           Infant, Newborn, Diseases [C16.614] +           Infant, Newborn, Diseases +

Congenital Abnormalities - Preferred

Concept UI	M0000013
Scope note	Malformations of organs or body parts during development in utero.
Preferred term	Congenital Abnormalities
Entry term(s)	Abnormalities, Congenital Abnormality, Congenital Birth Defect Birth Defects Congenital Abnormality Congenital Defect Congenital Defects Defect, Birth Defect, Congenital Defects, Birth Defects, Congenital Deformities Deformity

Fetal Anomalies - Related but not broader or narrower

Concept UI	M000677225
Preferred term	Fetal Anomalies
Entry term(s)	Anomaly, Fetal Fetal Anomaly

Fetal Malformations - Related but not broader or narrower

Concept UI	M000677226
Preferred term	Fetal Malformations
Entry term(s)	Fetal Malformation Malformation, Fetal