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