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 - Concepto preferido

UI del concepto	M0000013
Nota de alcance	Malformations of organs or body parts during development in utero.
Término preferido	Congenital Abnormalities
Término(s) alternativo(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