congenital
111congenital familial nonhemolytic jaundice — congenital nonhemolytic jaundice, Crigler Najjar jaundice Crigler Najjar syndrome …
112congenital generalized lipodystrophy — congenital progressive lipodystrophy total l …
113congenital abducens-facial paralysis — congenital oculofacial paralysis Mцbius syndrome …
114congenital photosensitive porphyria — congenital erythropoietic p …
115congenital trembles — congenital tremor syndrome …
116Congenital clasped thumb — Infant’s persistent thumb clutched hand,[1] flexion adduction deformity of the thumb,[2] pollex varus,[3] thumb in the hand deformity.[4] …
117congenital disorder — Structural abnormality (e.g., atresia, agenesis), functional problem (e.g., cystic fibrosis, phenylketonuria), or disease present at birth. Almost all are due to genetic factors (inherited or spontaneous mutations, chromosomal disorders),… …
118Congenital adrenal hyperplasia — CAH redirects here. For other meanings of CAH see CAH (disambiguation) Congenital adrenal hyperplasia Classification and external resources ICD 10 E25.0 ICD 9 …
119congenital heart disease — Deformity of the heart. Examples include septal defect (opening in the septum between the sides of the heart), atresia (absence) or stenosis (narrowing) of one or more valves, tetralogy of Fallot (with four components: ventricular septal defect,… …
120Congenital malformation — A physical defect present in a baby at birth, irrespective of whether the defect is caused by a genetic factor or by prenatal events that are not genetic. In a malformation, the development of a structure is arrested, delayed, or misdirected… …