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Metabolite Type:
All
Co-metabolite
Microbial
Human
Structure Class:
All
Indoles and derivatives
Biotin and derivatives
Organic sulfuric acids and derivatives
Host:
All
American dog tick
Birds
Cat
Catfish
Cattle
Chicken
Dog
Ferret
Fox
Freshwater
Goat
Himalayan marmot
Horse
House mouse
Human
Koala
Koalas (marsupials)
Lion
Llama
Mink
Pig
Pigeon
Primates
Rat
Relapsing fever tick
River trout
Sheep
Soil
Turkey
Wood mouse
Site:
All
skin
large intestine
small intestine
stomach
pharynx
oral cavity
nasal cavity
lower raspiratory tract
urinary tract
uterus
vagina
exocrine glands
CNS
Microbial Metabolism:
All
Saccharolytic
Consumption (import)
Production (export)
Macromolecule degradation
Consumption (import) (-)
Macromolecule degradation (-)
Production (export) (-)
Health Outcome:
All
healthy
1-Naphthol Exposure
11-beta-Hydroxylase deficiency
11-beta-hydroxylase deficiency
2,4,6-Trichlorophenol Exposure
2,4-Dichlorophenol Exposure
2,4-dienoyl-CoA reductase deficiency
2,5-Dimethylfuran Exposure
2-Aminoadipic aciduria
2-Ketoadipic Acidemia
2-Ketoglutarate Dehydrogenase Complex Deficiency
2-Ketoglutarate dehydrogenase complex deficiency
2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency (SBACDD)
2-Naphthol Exposure
21-Hydroxylase Deficiency (CYP21)
21-Hydroxylase deficiency
21-hydroxylase deficiency
27-hydroxylase deficiency
3-Hydroxy-3- methylglutaryl-CoA lyase (HL) deficency
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
3-Hydroxyacyl-CoA dehydrogenase deficiency (SCHAD)
3-Hydroxydicarboxylic aciduria
3-Hydroxyisobutyric Aciduria
3-Hydroxyisobutyric acid dehydrogenase deficiency
3-Hydroxyisobutyric aciduria
3-Hydroxyisobutyryl-coa hydrolase deficiency
3-Methyl-Crotonyl-Glycinuria
3-Methyl-crotonyl-glycinuria
3-Methylcrotonyl-CoA Carboxylase Deficiency
3-Methylglutaconic Aciduria (TYPE I)
3-Methylglutaconic Aciduria (TYPE II), X-LINKED
3-Methylglutaconic Aciduria (Type IV)
3-Methylglutaconic Aciduria (Type IX)
3-Methylglutaconic Aciduria (Type V)
3-Methylglutaconic Aciduria (Type VI)
3-Methylglutaconic Aciduria (Type VII)
3-Methylglutaconic aciduria type I
3-Phosphoglycerate Dehydrogenase Deficiency
3-hydroxy-3-methylglutaric aciduria
3-hydroxy-3-methylglutaric- coenzyme A lyase deficiency
3-methyl-crotonyl-glycinuria
3-methylglutaconic aciduria type I
3-methylglutaconic aciduria type II, X-linked
5-Oxoprolinase Deficiency
5-oxoprolinase deficiency
9-Hydroxyfluorene Exposure
ACTH deficiency, isolated
ADHD (Attention Defict Hyperactivity Disorder)
ADPKD
AIDS
Abetalipoproteinemia
Aceruloplasminemia
Active tobacco user
Active tobacco user
Acute Infantile Liver Failure
Acute ethanol intoxication
Acute intermittent porphyria
Acute lymphoblastic leukemia
Acute myelogenous leukemia (AML)
Acute or chronic demyelinating polyneuropathies
Acute promyelocytic leukemia (APL)
Acute seizures
Addison's disease
Adenosine deaminase (ADA) deficiency
Adenosine deaminase(ADA) deficiency
Adenosine kinase deficiency
Adenylosuccinase deficiency
Adenylosuccinate lyase deficiency
Adrenal Hypoplasia
Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency
Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency
Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete
Adrenoleukodystrophy
Adrenoleukodystrophy (ALD)
Adrenoleukodystrophy, X-linked
Adrenoleukodystrophy, neonatal
Adrenomyeloneuropathy
Alcohol abuse
Alcohol intoxication
Alcoholism
Alcoholism
Aldehyde dehydrogenase deficiency
Alkaptonuria
Allergic asthma
Alpha-1-antitrypsin deficiency
Alpha-Methylacyl-CoA racemase deficiency
Alpha-aminoadipic and alpha-ketoadipic aciduria
Alzheimer's Disease
Alzheimer's disease
Alzheimer's disease
Ambulant pregnancy
Aminoaciduria
Aminoacylase I deficiency
Aminoacylase I deficiency
Amish lethal microcephaly
Amyotrophic lateral sclerosis
Anemia
Anemia, congenital dyserythropoietic, type II
Anephrism
Anorexia nervosa
Anoxia
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
Apolipoprotein C-II deficiency
Apparent mineralocorticoid excess
Appendicitis
Arginase Deficiency
Argininemia
Argininemia
Argininosuccinic aciduria
Argininosuccinic aciduria (ASL)
Argininosuccinyl-CoA lyase deficiency
Aromatase deficiency
Aromatic L-amino acid decarboxylase deficiency
Aseptic meningitis
Aspartylglucosaminuria
Asthma
Asymptomatic acute intermittent porphyria
Asymptomatic acute intermittent porphyria (AIP)
Athyroic patients
Atrophic gastritis
Attachment loss
Autism
Autosomal dominant polycystic kidney disease (ADPKD)
Autosomal recessive spastic ataxia of Charlevoix-Saguena
Bacterial infections (assorted)
Bacterial meningitis
Bartter Syndrome, Type 1, Antenatal
Bartter Syndrome, Type 2, Antenatal
Bartter Syndrome, Type 3
Bartter Syndrome, Type 4A, Neonatal, with Sensorineural Deafness
Bartter Syndrome, Type 4B, Neonatal, With Sensorineural Deafness
Bartter Syndrome, Type 5, Antenatal, Transient
Beckwith-Wiedemann Syndrome
Benzene Exposure
Benzene exposure
Beta-mercaptolactate-cysteine Disulfiduria
Beta-thalassemia
Beta-ureidopropionase deficiency
Bilateral testicular adrenal rest tumors
Bile Acid Synthesis Defect, Congenital, 1
Biliary atresia
Biliary cirrhosis
Biotinidase deficiency
Bipolar disorder
Bladder cancer
Bladder infections
Bone metastases
Brain injury
Branched-chain Keto Acid Dehydrogenase Kinase Deficiency
Breast cancer
Breast cancer
Brown-Vialetto-Van Laere Syndrome 1
Brunner Syndrome
Bulimia Nervosa
CCD
CNS Infections
CNS Tumors
Cachexia
Cadmium Exposure
Cadmium exposure
Campylobacter jejuni infection
Canavan Disease
Canavan disease
Cancer - assorted types
Carbamoyl Phosphate Synthetase Deficiency
Carbamoyl phosphate synthetase deficiency
Carcinoid tumors
Cardiac arrest
Cardiopulmonary resuscitation
Cardiosvacular risk
Carnitine palmitoyltransferase deficiency I
Carnitine transporter defect; primary systemic carnitine deficiency
Carnitine-Acylcarnitine translocase deficiency
Carnitine-acylcarnitine translocase deficiency
Carnosinuria
Celiac Disease
Celiac disease
Cerebral Vasospasm
Cerebral creatine deficiency syndrome 1
Cerebral creatine deficiency syndrome 2
Cerebral creatine deficiency syndrome 3
Cerebral folate transport deficiency
Cerebral infarction
Cerebral infarction, headache, paresthesia and ununconfirmed suspicion of leucemic infaction or brain metastasis with normal CSF value
Cerebral infarction, headache, paresthesia and ununconfirmed suspicion of leucemic infaction or brain metastasis with normal CSF value but renal insufficiency
Cerebrocortical Degeneration
Cerebrotendinous xanthomatosis (CTX)
Cervical cancer
Cervical myelopathy
Cholangioma cancer
Cholecohal cyst
Cholestasis, progressive familial intrahepatic, 1
Cholesterol stones
Cholesteryl ester storage disease
Chondrodysplasia punctata, X-linked dominant
Chronic Renal Failure
Chronic active hepatitis
Chronic pancreatitis
Chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome
Chronic renal disease
Chronic renal failure
Cirrhosis
Cirrhosis
Citrullinemia Type I
Citrullinemia type II, adult-onset
Citrullinemia type II, neonatal-onset
Classicle Refsum's disease
Clostridium difficile infection
Clostridium difficile infection
Cobalamin A disease
Cobalamin C disease
Cobalamin Deficiency
Cobalamin F disease (cblF)
Cobalamin deficiency
Cobalamin malabsorption
Coenzyme Q10 deficiency
Coenzyme Q10 deficiency, primary, 1
Coenzyme Q10 deficiency, primary, 5
Colon cancer
Colorectal Cancer
Colorectal adenoma
Colorectal cancer
Combined D,L-2-hydroxyglutaric aciduria
Combined malonic and methylmalonic aciduria
Combined oxidative phosphorylation deficiency 10
Combined oxidative phosphorylation deficiency 11
Combined oxidative phosphorylation deficiency 12
Combined oxidative phosphorylation deficiency 14
Complex febrile seizures
Congenital Adrenal Hyperplasia, due to 21-Hydroxylase-Deficiency (CAH)
Congenital adrenal hyperplasia
Congenital cataracts, hearing loss, and neurodegeneration
Congenital chloride diarrhea
Congenital secretory diarrhea
Consuming polyphenols described by Phenol-Explorer entry
Consuming polyphenols described by Phenol-Explorer entry 414
Consuming polyphenols described by Phenol-Explorer entry 418
Consuming polyphenols described by Phenol-Explorer entry 420
Consuming polyphenols described by Phenol-Explorer entry 427
Consuming polyphenols described by Phenol-Explorer entry 429
Consuming polyphenols described by Phenol-Explorer entry 454
Consuming polyphenols described by Phenol-Explorer entry 572
Consuming polyphenols described by Phenol-Explorer entry 573
Consuming polyphenols described by Phenol-Explorer entry 579
Consuming polyphenols described by Phenol-Explorer entry 927
Consuming polyphenols described by Phenol-Explorer entry 928
Consuming polyphenols described by Phenol-Explorer entry 952
Consuming polyphenols described by Phenol-Explorer entry 953
Consuming polyphenols described by Phenol-Explorer entry 956
Consuming polyphenols described by Phenol-Explorer entry 961
Consuming polyphenols described by Phenol-Explorer entry 975
Consuming polyphenols described by Phenol-Explorer entry 983
Continuous ambulatory peritoneal dialysis (CAPD)
Convulsions
Coronary artery disease
Coronary heart disease
Corticosterone methyloxidase I deficiency- CMO I
Cotinine Exposure
Cresol poisoning
Crigler-Najjar syndrome Type I
Crohn disease
Crohn's Disease
Crohn's disease
Crohn's disease
Crohns disease
Cronh's ileitis
Cruetzfeldt-Jakob disease
Cryptococcus meningitis
Cryptosporidium infection
Cushing's syndrome
Cutis laxa, autosomal recessive, type IIIA
Cystathionine beta-synthase deficiency
Cystathioninuria
Cystic fibrosis
Cystinosis
Cystinuria
Cystinylglycinuria
Cytochrome C oxidase deficiency
D, L-2-hydroxygluraric aciduria
D, L-2-hydroxyglutaric aciduria
D,L-2-Hydroxyglutaric aciduria
D,L-2-hydroxyglutaric aciduria type I
D-2-Hydroxyglutaric aciduria
D-2-Hydroxyglutaric aciduria I
D-2-Hydroxyglutaric aciduria II
D-2-hydroxyglutaric aciduria
D-2-hydroxyglutaric aciduria type I
D-2-hydroxyglutaric aciduria type II
D-Bifunctional Protein Deficiency
D-Glyceric acidemia
D-Glyceric acidura
D-Lactic Acidosis
D-Lactic Acidosis and Short Bowel Syndrome
D2-/L2-hydroxyglutaric aciduria
Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome
Degenerative disc disease
Dementia
Dementia (Alzheimer's and non-Alzheimer's)
Dementia of Alzheimer type (DAT)
Dengue fever
Dental caries
Depersonalization syndrome
Depression
Dermal fibroproliferative disorder (hypertrophic scarring)
Desmosterolosis
Developmental Disorder Not Otherwise Specified
Diabetes
Diabetes
Diabetes Mellitus, Congenital Insulin-dependent, With Fatal Secretory Diarrhea; Immunodeficiency, Polyendocrinopathy, and Enteropathy, X-linked, Formerly
Diabetes and Deafness, Maternally Inherited
Diabetes mellitus
Diabetes mellitus type 2
Diarrhea-predominant IBS
Dibasic Amino Aciduria I
Dicarboxylic Aminoaciduria
Digeorge Syndrome
Dihydrolipoamide Dehydrogenase Deficiency
Dihydropyrimidinase deficiency
Dihydropyrimidine dehydrogenase (DPD) deficiency
Dimethyl sulfide poisoning
Dimethylglycinuria
Diverticular disease
Donohue Syndrome
Dopamine Beta-Hydroxylase Deficiency
Dopamine-serotonin Vesicular Transport Defect
Down syndrome pregnancy
Drunk driver
Duchenne Muscular Dystrophy
Early preeclampsia
Early-onset encephalopathy and cortical myoclonus (MECP2 gene mutation)
Eczema
Encephalitis
Endometrial cancer
Enterolactone Exposure
Enthesitis-related arthritis
Environmental enteric dysfunction
Eosinophilic esophagitis
Epilepsy
Epilepsy
Epilepsy, early-onset, vitamin B6-dependent
Epilepsy; Schizophrenia
Epileptic encephalopathy, early infantile, 39
Epithelial ovarian cancer
Essential hypertension
Ethanol Consumption
Ethanolaminuria
Ethylbenzene Exposure
Ethylene Glycol Poisoning
Ethylmalonic encephalopathy
Eucalyptol exposure
Extrahepatic biliary atresia (EHBA)
Fabry disease
Familial Mediterranean Fever
Familial amyotrophic lateral sclerosis
Familial lipoprotein lipase deficiency
Familial partial lipodystrophy
Fanconi Bickel syndrome
Fanconi syndrome
Fatal hydrogen sulfide poisoning
Fatty Acid Oxidation disorder with supplementation of MCT formula
Favorable outcome from traumatic brain injury
Febrile seizure
Folate Deficiency
Folate deficiency
Formic acid intoxication
Friedreich's ataxia
Frontotemporal lobe dementia
Fructose intolerance, hereditary
Fructose-1,6-bisphosphatase deficiency
Fulminant hepatic failure
Fumarase deficiency
Fumaric aciduria
Functional hypothalamic amenorrhea
GABA transaminase deficiency
GI disorder
GLUT1 deficiency syndrome
GOUT
GRACILE syndrome
Gaba-transaminase deficiency
Galactose-1-phosphate uridyltransferase deficiency (galactosemia)
Galactosemia
Galactosemia type 1
Gallstone disease
Gamma-Cystathionase deficiency
Gamma-glutamyltransferase deficiency
Gastroesophageal reflux disease
Generalized seizures
Genetically At-Risk of celiac disease
Genistein Exposure
Gestational diabetes mellitus (GDM)
Gitelman syndrome
Glucagon deficiency
Glucocorticoid resistance
Glucoglycinuria
Glucose transporter type 1 deficiency syndrome
Glucose-6-phosphate dehydrogenase deficiency
Glutamate formiminotransferase deficiency
Glutamine deficiency, congenital
Glutaric Aciduria II
Glutaric acidemia type 2
Glutaric aciduria I
Glutaric aciduria II
Glutaric aciduria type III
Glutaryl-CoA dehydrogenase deficiency (GDHD)
Glutathione synthetase deficiency
Glutathionuria
Glycerol Kinase Deficiency
Glycerol intolerance syndrom
Glycerol intolerance syndrome
Glycerol kinase deficiency
Glycine N-Methyltransferase deficiency
Glycogen storage disease
Glycolic aciduria
Gout
Growth hormone deficiency
Guillain-Barre syndrome (GBS)
Gynecological diseases (benign)
HIV and diarrhea
Hartnup Disease
Hawkinsinuria
Head injury
Head trauma
Heart Transplant
Heart failure
Heart failure with preserved ejection fraction
Heart failure with reduced ejection fraction
Heat Stress
Heat stress
Hemodialysis
Hemodialysis
Hemodialysis patients with colon
Hemodialysis patients with colons
Hemodialysis patients without colons
Hepatic and biliary malignancies
Hepatic coma (fatal)
Hepatic encephalopathy
Hepatitis
Hepatobiliary Disease
Hepatocellular cancer
Hepatocellular carcinoma
Hepatocellular carcinoma
Hereditary coproporphyria
Hereditary folate malabsorption
Hereditary tyrosinemia
Hirsutism
Histidinemia
Histidinuria
Homocystinuria
Homocystinuria due to defect of N(5,10)-methylene THF deficiency
Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type
Homogentisic Acid Oxidase deficiency (Alkaptonuria)
Homozygous sickle cell disease
Huntington's disease
Hydrocephalus
Hydrogen sulfide fatal poisoning
Hydroxylysinuria
Hydroxyprolinemia
Hyper beta-alaninemia
Hyperammonemia
Hyperargininemia
Hypercholesterolemia
Hypercholesterolemia, familial
Hyperdibasic aminoaciduria I
Hyperekplexia
Hyperglycinaemia
Hyperglycinemia, lactic acidosis, and seizures
Hyperinsulinemic hypoglycemia, familial, 1, HHF1
Hyperinsulinism-hyperammonemia syndrome
Hyperlipidaemia
Hyperlipidemia
Hyperlysinemia I, familial
Hyperlysinemia II or Saccharopinuria
Hyperlysinuria
Hypermanganesemia with dystonia 1
Hypermanganesemia with dystonia 2
Hypermethioninemia
Hyperornithinemia with gyrate atrophy
Hyperornithinemia–Hyperammonemia-Homocitrullinuria syndrome
Hyperoxalemia
Hyperphenylalaninemia due to 6-pyruvoyltetrahydropterin synthase deficiency (PTPS)
Hyperphenylalaninemia due to guanosine triphosphate cyclohydrolase deficiency
Hyperphenylalaninemia due to pterin-4a-carbinolamine dehydratase
Hyperphosphatasia
Hyperpipecolatemia
Hyperprolinemia, type I
Hyperprolinemia, type II
Hypertension
Hypertension (mild)
Hyperthyroidism
Hypervalinemia
Hyperzincaemia and Hypercalprotectinaemia
Hypoadrenocorticism
Hypobetalipoproteinemia
Hypoglycemia, familial neonatal
Hypogonadism
Hypomagnesemia 1, intestinal
Hypoparathyroidism-retardation-dysmorphism syndrome
Hypophosphatasia, infantile
Hypothyroidism
Hypothyroidism
Hypothyroidism, congenital, nongoitrous, 2
Hypoxia/Ischemia
Hypoxic-ischemic encephalopathy
Idiopathic intracranial hypertension
Idiopathic neonatal hepatitis
Idiopathic oro-facial pain
Idiopathic polyneuritis
Ileal Crohn's disease
Ileocysoiplasty
Iminoglycinuria
Immunoglobulin A nephropathy
Immunoglobulin A nephropathy (IgAN) non progressor
Immunoglobulin A nephropathy (IgAN) progressor
Impaired glucose tolerance
Infantile Liver Failure Syndrome 2
Infantile Refsum disease
Infantile Refsum's disease
Inflammatory bowel disease
Insulin-dependent diabetes mellitus(IDDM)
Interstitial cystitis
Intestinal infections
Intracranial tumours
Intrahepatic biliary hypoplasia
Intraventricular hemorrhage
Invasive candidiasis
Iron Deficiency
Irritable Bowel Syndrome
Irritable bowel syndrome
Irritable bowel syndrome (IBS)
Ischemic heart disease
Isobutyryl-CoA Dehydrogenase Deficiency
Isolated 3-Methylcrotonyl-CoA Carboxylase Deficiency
Isopropyl alcohol poisoning
Isovaleric acidemia
Isovaleric acidemia
Juvenile myoclonic epilepsy (JME)
Ketosis
Ketotic hypoglycemia
Kidney Cancer
Kidney cancer
Kidney disease
Kynureninase deficiency
L-2-Hydroxyglutaric aciduria
L-2-hydroxyglutaric aciduria
Lactose Intolerance
Late-onset preeclampsia
Lathosterolosis
Lead Exposure
Leber Optic Atrophy and Dystonia
Lecithin:cholesterol Acyltransferase Deficiency
Leigh Syndrome
Leigh Syndrome, French Canadian Type
Leptin Deficiency or Dysfunction
Lesch-Nyhan syndrome
Lesch-Nyhan syndrome
Leukemia
Leukoencephalopathy and peripheral neuropathy
Leukotriene C4-Synthesis Deficiency
Lewy body disease
Lipodystrophy
Lipodystrophy, Congenital Generalized
Lipoid Adrenal Hyperplasia
Lipoyltransferase 1 Deficiency
Liver Cirrhosis
Liver disease
Liver disease (encephalopathic)
Liver disease (non-encephalopathic)
Liver dysfunction
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Long-chain Fatty Acids, Defect in Transport of
Lung cancer
Lysinuric protein intolerance
Lysinuric protein intolerance (LPI) syndrome
Macular degeneration
Major affective disorder
Major depression
Major trauma
Malaria
Malignant melanoma or sarcoma
Malnutrition (type kwashiorkor and marasmus)
Malonyl-CoA decarboxylase deficiency
Malonyl-Coa decarboxylase deficiency
Mania
Maple syrup urine disease
Maple syrup urine disease
Maple syrup urine disease (MSUD)
Maple syrup urine disease (MSUD). When treated, the concentrations are 1-2 uM/mM.
Mastocytosis
Maturity onset diabetes of the young, type 2
Meckels diverticulum
Medium Chain Acyl-CoA Dehydrogenase Deficiency
Medium chain acyl-CoA dehydrogenase deficiency (MCAD)
Meningitis
Meningitis
Meningomyelocoele
Menkes syndrome
Menstrual cycle
Menstrual cycle
Menstrual cycle (follicular phase)
Menstrual cycle (luteal phase)
Menstrual cycle (midcycle)
Mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma
Mercury Exposure
Metabolic Disorder
Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration
Metastatic melanoma
Methamphetamine (MAP) psychosis
Methanol poisoning
Methionine adenosyltransferase (MAT) I/III deficiency
Methionine adenosyltransferase deficiency
Methotrexate treatment
Methyl Formate Exposure
Methyl formate exposure
Methylenetetrahydrofolate reductase deficiency
Methylmalonate semialdehyde dehydrogenase deficiency
Methylmalonic acidaemia
Methylmalonic aciduria mitochondrial encephelopathy Leigh-like
Methylmalonic aciduria, cblA type
Methylmalonic aciduria, cblB type
Methylmalonyl-CoA mutase deficiency
Mevalonic aciduria
Mild cognitive impairment
Missing teeth
Mitochondrial Myopathy, Infantile, Transient
Mitochondrial complex I deficiency due to ACAD9 deficiency
Mitochondrial encephalomyopaththy with elevanted methylmalonic acid, SUCLA2
Mitochondrial phosphate carrier deficiency
Mitochondrial pyruvate carrier deficiency
Mitochondrial trifunctional protein deficiency
Mitochondrial-encephalopathy-lactic acidosis-stroke
Molybdenium co-factor deficiency
Molybdenum Exposure
Molybdenum cofactor deficiency
Monocarboxylate transporter 1 deficiency
Morphine treatment
Motor neuron disease (MND)
Mucopolysaccharidosis IVA
Multiple Sclerosis
Multiple System Atrophy (MSA)
Multiple acyl-CoA dehydrogenase deficiency
Multiple carboxylase deficiency
Multiple sclerosis
Multiple sclerosis
Myalgic encephalomyelitis/chronic fatigue syndrome
Mycobacterium tuberculosis
Myocardial infarction
Myoclonic epilepsy and ragged red fiber disease
Myopathic carnitine deficiency
Myopathy with lactic acidosis, hereditary
Myopathy, lactic acidosis, and sideroblastic anemia 1
N-Acetylglutamate synthetase deficiency
N-acetylglutamate synthetase deficiency
N/A
NULL
Narcolepsy
Narp Syndrome
Neonatal adrenoleukodystrophy
Nephrotic syndrome
Neu-Laxova Syndrome 1
Neuroborreliosis
Neurodegenerative diseases
Neuroinfection
Nicotinamide Adenine Dinucleotide Deficiency
Nitrate Exposure
Non-insulin dependent diabetes
Non-ketotic hyperglycinemia
Nonalcoholic fatty liver disease
Nonalcoholic fatty liver disease (NAFLD)
Nonketotic Hyperglycinemia
Normal
Normal
Normal
Nucleotide Depletion Syndrome
OTC-deficiency
Obese
Obesity
Occipital Horn Syndrome
Oculocerebrorenal Syndrome of Lowe
Odontohypophosphatasia
Olivopontocerebellar atrophy (OPCA)
Oral cancer
Oral leukoplakia (OLK)
Oral squamous cell carcinoma (OSCC)
Ornithine transcarbamylase (OTC) deficiency
Ornithine transcarbamylase deficiency
Orotic Aciduria hereditary
Orotic aciduria I
Osteoarthritis
Osteoporosis
Ovarian cancer
Overweight
PNPO deficiency
Pancreatic cancer
Pancreatic ductal adenocarcinoma
Panic Disorder
Paraquat Poisoning
Paraquat poisoning
Parkinson's Disease
Parkinson's disease
Parkinson's disease with motor fluctuation
Parkinson's disease without motor fluctuation
Parkinson's syndrome
Partial lipodystrophy
Patent Ductus Venosus
Pearson Syndrome
Pelizaeus Merzbacher Disease
Pellagra
Pendred Syndrome
Pentachlorophenol Exposure
Pentosuria
Perchloroethylene Exposure
Perillyl alcohol administration for cancer treatment
Periodontal Probing Depth
Periodontal diseases
Peripheral Neuropathy
Peripheral arterial disease
Peripheral neuropathy
Peritoneal dialysis
Permanent Intestinal Failure
Permanent intestinal failure
Peroxisomal biogenesis defect
Peroxisomal biogenesis disorder
Peroxisomal disorders, new type, liver
Pervasive Developmental Disorder Not Otherwise Specified
Phenylketonuria
Phenylketonuria
Pheochromocytoma
Pheochromocytoma
Phosphoenolpyruvate Carboxykinase Deficiency 1, Cytosolic
Phosphoribosylpyrophosphate Synthetase Superactivity
Phosphoserine Aminotransferase Deficiency
Phosphoserine Phosphatase Deficiency
Phytosterolemia
Pituitary Hormone Deficiency, Combined, 1
Polycystic ovary syndrome (PCOS)
Porphyria
Porphyria cutanea tarda
Porphyria variegata
Portal vein obstruction
Postoperative pulmonary hypertension
Postpartum depression
Prader-Willi syndrome
Preeclampsia
Pregnancy
Pregnancy with fetus having congenital heart defect
Pregnancy with fetuses with trisomy 18
Pregnene hydroxylation deficiency
Premature
Premature neonates
Premenstrual dysphoric disorder (follicular stage of menstrual cycle)
Premenstrual dysphoric disorder (late luteal stage of menstrual cycle)
Premenstrual dysphoric disorder (mid luteal stage of menstrual cycle)
Prepartum depression
Preterm birth
Preterm infants
Primary Hyperoxaluria II, PH2
Primary Hypomagnesemia
Primary biliary cirrhosis
Primary hyperoxaluria I
Primary hypertension
Primary hypomagnesemia
Progressive cognitive impairment
Progressive dementia
Progressive supranuclear palsy
Prolactinoma
Prolidase deficiency
Propionic acidemia
Propionic acidemia
Proprotein Convertase 1/3 Deficiency
Prostate Cancer
Prostate cancer
Prosthesis/Missing teeth
Proteinuria
Protoporphyria, Erythropoietic
Pseudo Zellweger->D-bifunctional protein deficiency
Pseudohypoaldosteronism, type I, autosomal dominant
Pseudoneonatal adrenoleukodystrophy
Psychiatric disorder
Purine nucleoside phosphorylase (PNP) deficiency
Purine nucleoside phosphorylase (PNP) deficiency
Purine nucleoside phosphorylase deficiency
Pyridoxamine 5-prime-phosphate oxidase deficiency
Pyridoxine dependency with seizures (PDE)
Pyruvate carboxylase deficiency
Pyruvate dehydrogenase deficiency
Pyruvate dehydrogenase deficiency (E1)
Pyruvate dehydrogenase deficiency E1-alpha
Pyruvate dehydrogenase phosphatase deficiency
Rachialgia
Recurrent Clostridium difficile infection
Refractory localization-related epilepsy (RLE)
Refsum disease, classic, adult-onset
Refsum disease, classic, early-onset
Refsum disease, infantile
Refsum disease, juvenile
Refsum's Disease
Refsum's disease
Renal fanconi syndrome
Renal tubular acidosis, distal, RTA type 1
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation
Retarded depression
Rett syndrome
Reye's Syndrome
Rhabdomyolysis
Rheumatoid arthritis
Rheumatoid arthritis
Rhinitis
Rhizomelic chondrodysplasia punctata
Ribose-5-Phosphate Isomerase Deficiency
Ribose-5-phosphate isomerase deficiency
Roofers (post shift)
S-Adenosylhomocysteine hydrolase deficiency
SC4MOL deficiency
SIALIDOSIS, normosomatic type
Salla disease
Sarcosinemia
Schizophrenia
Schizophrenia
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SESAMES)
Sengers syndrome
Sepiapterin Reductase Deficiency
Sepsis
Septic shock
Serine deficiency syndrome, infantile
Severe acute malnutrition
Severe vascular dementia
Short Chain Acyl-Coa Dehydrogenase Deficiency
Short bowel syndrome
Short chain acyl-CoA Dehydrogenase deficiency (SCAD)
Short chain acyl-CoA dehydrogenase deficiency (SCAD)
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
Sickle cell anemia
Sickle cell disease-SS (SCD-SS)
Sildenafil-induced headache
Simple febrile seizures
Sitosterolemia
Sjögren-Larsson syndrome
Small intestinal bacterial overgrowth
Small intestinal malabsorption, HIV, & cryptosporidiosis
Small intestinal malabsorption, HIV, & diarrhea
Small intestinal malabsorption, scleroderma, & bacterial overgrowth
Smith-Lemli-Opitz syndrome
Smoking
Sodium Nitrate Consumption
Sodium nitrate consumption
Solid tumors
Soy consumption (ileostomies)
Spina bifida
Spondyloenchondrodysplasia
Sporadic amyotrophic lateral sclerosis
Stomach cancer
Stress period
Stroke
Styrene Exposure
Subarachnoid Aneurysmal Hemorrhage
Subarachnoid haemorrhage
Subarachnoid hemorrhage
Succinic semialdehyde dehydrogenase deficiency
Succinyl CoA: 3-ketoacid CoA transferase deficiency
Sucrase-isomaltase deficiency
Sulfite oxidase deficiency
Sulphite oxidase deficiency
Supradiaphragmatic malignancy
Supragingival Calculus
Supragingival Plaque
Taking drug identified by DrugBank entry
Temporomandibular joint disorder (TMD)
Tert Amyl Methyl Ether Exposed
Thiocyanate Exposure
Thymidine phosphorylase deficiency
Thyroid cancer
Thyroid cancer
Tic disorder
Toluene Exposure
Tooth Decay
Tooth alignment disorders
Transaldolase deficiency
Transaldolase deficiency
Transaldolase deficiency
Transcobalamin II deficiency
Transient wheezing
Transurethral prostatectomy syndrome
Trauma
Traumatic Brain Injury (TBI)
Traumatic brain injury
Traumatic brain injury (TBI)
Treated celiac disease
Triclosan Exposure
Trimethylaminuria
Tryptophanuria with dwarfism
Tuberculosis
Tuberculous meningitis
Type 1 diabetes Mellitus
Type 2 Diabetes
Type I diabetes
Typical pyridoxine-dependent seizures
Tyrosinemia I
Tyrosinemia I
Ulcerative Colitis
Ulcerative colitis
Ulcerative colitis
Unclassified IBD
Uremia
Urocanase deficiency
Vascular Dementia
Vascular dementia
Vascular dementia
Very long-chain acyl-CoA dehydrogenase deficiency (vLCAD)
Viral Infection
Viral infections (assorted)
Vitamin B12 deficiency
Vitamin E deficiency
Vitiligo
Wilson's disease
Wolcott-Rallison syndrome
Wolfram syndrome 1
Woodhouse-Sakati syndrome
X-linked adrenoleukodystrophy
X-linked ichthyosis
Xanthinuria type 1
Xanthinuria type II
Zellweger Syndrome
Zellweger syndrome
adult-type citrullinemia
alpha-Aminoadipic aciduria
alpha-Ketoadipic Aciduria
alpha-ketoadipic aciduria
amyotrophic lateral sclerosis
ankylosing spondylitis
anorexia
argininemia
asymptomatic diverticulosis
autism
beta-Mannosidosis
celiac disease
cobalamin deficiency
congenital disorder of glycosylation CDG-Ia
depressive
fibromyalgia
gastric cancer
glutathione synthetase deficiency, acute metabolic crisis
hydrocephalus
hypothyroidism
ischaemic stroke
isovaleric acidemia
juvenile idiopathic arthritis
leukemia
meningitis
multiple carboxylase deficiency
multiple sclerosis
non-Clostridium difficile diarrhea
normal
o-Xylene Exposure
pheochromocytoma
propionic acidemia
rheumatoid arthritis
sepiapterin reductase deficiency
severe traumatic brain injury (TBI)
symptomatic uncomplicated diverticular disease
tert-Amyl-methyl ether exposed
uremia
Biospecimen:
All
Blood
Urine
Saliva
Cerebrospinal Fluid
Feces
Sweat
Breast Milk
Bile
Amniotic Fluid
Other Biospecimens
Status in Biospecimen:
All
Detected and Quantified
Detected but not Quantified
Expected but not Quantified
Predicted
Bioactivity:
All
Uremic toxin
amnesia
cytotoxic
hepatitis
Exposure Source:
All
Endogenous
Food
Animal
Plant
Environment
Clear
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Metabolite ID
Name
Molecular Formula
Average Mass
Monoisotopic Mass
Structure
Structure Class
Host and Biospecimen
# Microbes
Metabolite Type
Exposure Sources
Health Effects
Detection Status
MMDBc0008352
Tricycloalternarene 5b
C
22
H
32
O
3
344.495
344.23514489
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0009373
Tricycloalternarene 6a
C
21
H
32
O
5
364.482
364.22497413
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0012757
Tricycloalternarene 6b
C
21
H
32
O
5
364.482
364.22497413
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0011353
Tricycloalternarene 7a
C
22
H
34
O
5
378.509
378.240624195
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0006481
Tricycloalternarene 7b
C
22
H
34
O
5
378.509
378.240624195
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0013873
Tricycloalternarene 8a
C
21
H
30
O
4
346.467
346.214409446
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0007734
Tricycloalternarene 9b
C
21
H
30
O
3
330.468
330.219494826
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0009988
Tricycloalternarene A
C
18
H
24
O
5
320.385
320.162373873
Fatty Acyls
Not Available
2
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0011650
Tricycloalternarene B
C
23
H
32
O
5
388.504
388.22497413
Prenol lipids
Not Available
2
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0001284
Tricycloalternarene D
C
23
H
34
O
5
390.52
390.240624195
Organooxygen compounds
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0016346
Tricycloalternarene E
C
21
H
32
O
5
364.482
364.22497413
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0027449
Tricycloalternarene K
C
21
H
30
O
5
362.466
362.209324066
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0027448
Tricycloalternarene L
C
18
H
24
O
5
320.385
320.162373873
Fatty Acyls
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0033072
tridecaprenyl diphosphate
C
65
H
108
O
7
P
2
1063.4963
1062.757028834
Prenol lipids
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0030362
Triethanolamine
C
6
H
15
NO
3
149.1882
149.105193351
Organonitrogen compounds
Human Placenta
Human Sweat
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0056343
triglucosyl-enterobactin
C
48
H
57
N
3
O
30
1155.975
1155.302687447
Peptidomimetics
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0000553
Trigonelline
C
7
H
7
NO
2
137.136
137.047678473
Human Urine
Human Placenta
Human Blood
Human Feces
6
Co-metabolite
Plant
Lung Cancer
; Eosinophilic esophagitis
Detected and Quantified
MMDBc0000168
Trimethylamine
C
3
H
9
N
59.1103
59.073499293
Organonitrogen compounds
Human Urine
Human Cerebrospinal Fluid (CSF)
Human Saliva
Human Blood
Human Feces
Human Epidermis
Human Skeletal Muscle
199
Co-metabolite
Milk
Dimethylglycine Dehydrogenase Deficiency
; Kidney disease
; Trimethylaminuria
; Trimethylaminuria
; Trimethylaminuria
; Uremia
; Eosinophilic esophagitis
Detected and Quantified
MMDBc0000169
Trimethylamine N-oxide
C
3
H
9
NO
75.1097
75.068413915
Organonitrogen compounds
Human Urine
Human Saliva
Human Blood
Human Feces
Human Cerebrospinal Fluid (CSF)
Human Epidermis
Human Kidney
Human Liver
Human Placenta
146
Co-metabolite
Milk
Argininosuccinic aciduria
; Dimethylglycine Dehydrogenase Deficiency
; Kidney disease
; Lung Cancer
; Maple syrup urine disease
; Propionic acidemia
; Rhabdomyolysis
; Trimethylaminuria
; Trimethylaminuria
; Tyrosinemia I
; Uremia
; Eosinophilic esophagitis
Detected and Quantified
MMDBc0017830
Trimethylpyrazine
C
7
H
10
N
2
122.1677
122.08439833
Diazines
Not Available
2
Co-metabolite
Fruit
Not Available
Detected and Quantified
MMDBc0033146
Trimyristin
C
45
H
86
O
6
723.1607
722.642440484
Not Available
1
Co-metabolite
Milk
Not Available
Detected and Quantified
MMDBc0029710
Triphosphate
O
10
P
3
252.9153
252.870430756
Non-metal oxoanionic compounds
Human Feces
884
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0017260
Trisindoline
C
24
H
17
N
3
O
363.42
363.137162179
Not Available
1
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0031947
tRNA(Ala)
C
10
H
18
O
9
282.245
282.09508216
Organooxygen compounds
Human Feces
2
Co-metabolite
Not Available
Not Available
Detected and Quantified
MMDBc0034218
Tropic acid
C
9
H
10
O
3
166.1739
166.062994186
Not Available
2
Co-metabolite
Milk
Not Available
Detected and Quantified
Displaying metabolites
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