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Term:
bilirubin metabolic disorder
(DOID:2741)
Annotations:
Rat: (69)
Mouse: (62)
Human: (68)
Chinchilla: (45)
Bonobo: (51)
Dog: (53)
Squirrel: (48)
Pig: (52)
Parent Terms
Term With Siblings
Child Terms
inherited metabolic disorder
+
Pathologic Processes
+
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
3-Hydroxyacyl-CoA Dehydrogenase Deficiency
3-methylglutaconic aciduria
+
5-Nucleotidase Syndrome
6-Phosphogluconolactonase Deficiency
Acantholysis
+
aceruloplasminemia
Acetylcarnitine Deficiency
Acholinesterasemia
Acid Phosphatase Deficiency
Acute Reversible Leukoencephalopathy with Increased Urinary Alpha-ketoglutarate
Alpha-Fetoprotein Deficiency
amino acid metabolic disorder
+
Amino Acid Transport Disorders, Inborn
+
Angiotensin I-Converting Enzyme, Benign Serum Increase
Arene Oxide Detoxification Defect
aromatase excess syndrome
Aryl Hydrocarbon Hydroxylase Inducibility
Ascites
Atrial Remodeling
Azotemia
bilirubin metabolic disorder
+
An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism. (DO)
Butyrylcholinesterase Deficiency
Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type
carbohydrate metabolic disorder
+
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO
Cardiac Arrhythmias
+
Cardiotoxicity
+
Carnitine Acetyltransferase Deficiency
cerebral amyloid angiopathy
+
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
DYSOSTOSIS MULTIPLEX, AIN-NAZ TYPE
Efavirenz, Poor Metabolism of
Emphysema
+
enterokinase deficiency
Ethanolaminosis
Extravasation of Diagnostic and Therapeutic Materials
Familial Amyloidosis
+
familial erythrocytosis 8
familial hypocalciuric hypercalcemia
+
Familial Hypokalemia
+
Femoracetabular Impingement
Fibrosis
+
FUCOSYLTRANSFERASE 6 DEFICIENCY
Genomic Instability
+
Gliosis
Glucocorticoid Receptor Deficiency
Glucose-Stimulated Secretory Diarrhea, with Common Variable Immunodeficiency
Glycoprotein Storage Disease
Glyoxalase II Deficiency
Gordon Holmes syndrome
Granuloma
+
Greenberg dysplasia
Growth Disorders
+
Hemolysis
+
Hemorrhage
+
Hereditary Hyperbilirubinemia
+
Heterotopic Ossification
+
Hyperammonemia
+
Hyperamylasemia
Hypercalcemia, Infantile, 1
hyperphosphatemic familial tumoral calcinosis
+
Hyperplasia
+
hyperuricemia
+
Hypoadiponectinemia
hypoinsulinemic hypoglycemia with hemihypertrophy
Hypovolemia
immunodeficiency 43
immunoglobulin light chain amyloidosis
Inflammation
+
Inosine Triphosphatase Deficiency
Intraoperative Complications
+
ischemia
+
isolated elevated serum creatine phosphokinase levels
isolated hyperchlorhidrosis
Kallikrein, Decreased Urinary Activity of
Lactate Dehydrogenase B Deficiency
Lactic Aciduria due to D-Lactic Acid
Leptin Receptor Deficiency
Leukoaraiosis
Leukocytosis
+
Leukotriene C4 Synthase Deficiency
lipid metabolism disorder
+
Lithiasis
Long Term Adverse Effects
lysosomal storage disease
+
Malacoplakia
+
Malonic Aciduria
Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type
Mannose-Binding Protein Deficiency
maturity-onset diabetes of the young
+
Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency
Menstruation Disturbances
+
Metabolic Brain Diseases, Inborn
+
metal metabolism disorder
+
Metaplasia
+
Methemoglobin Reductase Deficiency
Methylmalonyl-Coenzyme A Mutase Deficiency
mitochondrial metabolism disease
+
MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY
Monocarboxylate Transporter 1 Deficiency
Monocyte Esterase Deficiency
Muscle Weakness
+
Myeloperoxidase Deficiency
Myotoxicity
N Acetyltransferase Deficiency
+
Necrosis
+
Neointima
neonatal diabetes mellitus with congenital hypothyroidism
Neoplastic Processes
+
Nerve Degeneration
+
Nonfunctional L-Gulonolactone Oxidase
Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase Deficiency
Nonspherocytic Hemolytic Anemia, due to Hexokinase Deficiency
ochronosis
+
Orofacial Granulomatosis
overhydrated hereditary stomatocytosis
permanent neonatal diabetes mellitus
+
peroxisomal disease
+
Phenacetin O-Deethylase, Deficiency of
Phenol Sulfotransferase Deficiency
phosphoglycerate kinase 1 deficiency
Phosphohydroxylysinuria
pigmentation disease
+
plasma protein metabolism disease
+
Polydipsia
+
Poor Drug Metabolism, CYP2C19-Related
Poor Drug Metabolism, CYP2D6-Related
Poor Metabolism of Proguanil
porphyria
+
Postoperative Complications
+
progeria
+
Protein Aggregation, Pathological
purine-pyrimidine metabolic disorder
+
pyrimidine metabolic disorder
+
renal tubular transport disease
+
Respiratory Aspiration
+
Retinol-Binding Protein Deficiency
Retropneumoperitoneum
Sclerosis
+
SEDOHEPTULOKINASE DEFICIENCY
sepiapterin reductase deficiency
Shock
+
Squalene Synthase Deficiency
steroid inherited metabolic disorder
+
Stomatocytosis II
Succinic Acidemia
SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY
Teratogenesis
Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type)
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type)
thiopurine S-methyltransferase deficiency
+
Thyrotropin-Releasing Hormone Deficiency
Transcobalamin I Deficiency
trimethylaminuria
Trypsinogen Deficiency
type 1 diabetes mellitus 2
Ulcer
+
Uridine-Cytidineuria
variant ABeta2M amyloidosis
Vascular Remodeling
+
vitamin metabolic disorder
+
warfarin resistance
warfarin sensitivity
+
Weinstein Kliman Scully Syndrome
Wiedemann Oldigs Oppermann Syndrome
Yang Deficiency
Yin Deficiency
Crigler-Najjar syndrome
+
Dubin-Johnson syndrome
Gilbert syndrome
Hereditary Hyperbilirubinemia
+
Jaundice
+
kernicterus
+
Neonatal Hyperbilirubinemia
+
Synonyms
Exact Synonyms:
bilirubinemia ; bilirubinemias ; hyperbilirubinaemia ; hyperbilirubinemia ; hyperbilirubinemias
Primary IDs:
MESH:D006932
Xrefs:
NCI:C84761
;
OMIM:PS237450
Definition Sources:
http://en.wikipedia.org/wiki/Hereditary_hyperbilirubinemia
"DO" "DO"