familial nonhemolytic jaundice
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congenital familial nonhemolytic jaundice — congenital nonhemolytic jaundice, Crigler Najjar jaundice Crigler Najjar syndrome … Medical dictionary
Jaundice — Yellowish staining of the skin and sclerae (the whites of the eyes) by abnormally blood high levels of the bile pigment bilirubin. The yellowing extends to other tissues and body fluids. Jaundice was once called the morbus regius (the regal… … Medical dictionary
Icterus — Jaundice. At least one medical dictionary defines icterus as the presence of jaundice seen in the sclera of the eye. This is incorrect. Icterus is synonymous with jaundice. They are one and the same thing. Curiously, both icterus and jaundice… … Medical dictionary
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
Síndrome de Crigler-Najjar — Molécula de bilirrubina. Clasificación y recursos externos CIE 10 E80.5 … Wikipedia Español
Dysfunction — Difficult function or abnormal function. There is, for example: Constitutional hepatic dysfunction, (familial nonhemolytic jaundice), Dental dysfunction (abnormal functioning of dental structures), Minimal brain dysfunction (attention deficit… … Medical dictionary
Crigler–Najjar syndrome — Classification and external resources Bilirubin ICD 10 E80.5 … Wikipedia
Crigler-Najjar syndrome — DiseaseDisorder infobox Name = Crigler Najjar Syndrome ICD10 = ICD10|E|80|5|e|70 ICD9 = ICD9|277.4 ICDO = Caption = Bilirubin OMIM = 218800 OMIM mult = OMIM2|606785 MedlinePlus = 001127 eMedicineSubj = med eMedicineTopic = 476 DiseasesDB = 3176… … Wikipedia
Gilbert syndrome — A common but harmless genetic condition in which a liver enzyme essential to the disposal of bilirubin (the chemical that results from the normal breakdown of hemoglobin from red blood cells) is abnormal. This enzyme abnormality results in mild… … Medical dictionary
