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 Anencephaly [C16.131.085.197] Anencephaly Twins, Conjoined [C16.131.085.806] Twins, Conjoined 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

Abnormalities, Severe Teratoid - Conceito preferido

Identificador do conceito	M0014046
Nota de escopo	Marked developmental anomalies of a fetus or infant.
Termo preferido	Abnormalities, Severe Teratoid
Termo(s) alternativo(s)	Abnormality, Severe Teratoid Severe Teratoid Abnormalities Severe Teratoid Abnormality Teratoid Abnormalities, Severe Teratoid Abnormality, Severe