A condition characterized by an abnormal increase of BILIRUBIN in the blood, which may result in JAUNDICE. Bilirubin, a breakdown product of HEME, is normally excreted in the BILE or further catabolized before excretion in the urine.
Butyrylcholinesterase Deficiency
Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type
carbohydrate metabolic disorder +
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO
Cardiac Arrhythmias +
Cardiotoxicity +
Carnitine Acetyltransferase Deficiency
Channelopathies +
CHITOTRIOSIDASE DEFICIENCY
Chromate Resistance
Chromosome Aberrations +
Combined Congenital Deficiency of Intrinsic Factor and R Binder
Combined Defect of Growth Factors
Combined Exocrine Pancreatic Insufficiency
Combined Immunodeficiency and Megaloblastic Anemia with or without Hyperhomocysteinemia
congenital leptin deficiency
congenital secretory chloride diarrhea 1
congenital secretory sodium diarrhea 3
Copper Deficiency, Familial Benign
Coumarin Sensitivity
cytochrome-c oxidase deficiency disease +
Deafness Hyperuricemia Neurologic Ataxia
Death +
Defect in Hyaluronan Metabolism
Defect in Hydroxylation of Diphenylhydantoin
Deficient N-Hydroxylation of Amobarbital
Dehydration
Delayed Graft Function
Deoxyribose-5-Phosphate Aldolase Deficiency
Disease Attributes +
dopamine beta-hydroxylase deficiency
Dysbiosis
Efavirenz, Poor Metabolism of
Emphysema +
enterokinase deficiency
Ethanolaminosis
Extravasation of Diagnostic and Therapeutic Materials
Familial Amyloidosis +
familial erythrocytosis 8
Familial Hypokalemia
Femoracetabular Impingement
Fibrosis +
FUCOSYLTRANSFERASE 6 DEFICIENCY
Genomic Instability +
Gliosis
Glucocorticoid Receptor Deficiency
Glucose-Stimulated Secretory Diarrhea, with Common Variable Immunodeficiency