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Ontology Browser
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
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 

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"

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