more general categories
information about this item
1. Human Genes
1. Human Genes
solute carrier family 06 (neurotransmitter transporter), member 03 [HGNC:SLC6A3] (47)
solute carrier family 06 (neurotransmitter transporter), member 04 [HGNC:SLC6A4] (41)
solute carrier family 18 (vesicular monoamine transporter), member 2 [HGNC:SLC18A2] (16)
2. Interaction: Human Genes and Chemicals
2. Interaction: Human Genes and Chemicals
binding (2423)
cotreatment (1499)
activity (2549)
reaction (3393)
response to substance (713)
response to substance (641)
uptake (378)
C04. Neoplasms
C04. Neoplasms
Ependymoma [MESH:D004806] (76)
Oligodendroglioma [MESH:D009837] (241)
Glioblastoma [MESH:D005909] (2554)
Pheochromocytoma [MESH:D010673] (275)
Ependymoma [MESH:D004806] (76)
Oligodendroglioma [MESH:D009837] (241)
Glioblastoma [MESH:D005909] (2554)
Ependymoma [MESH:D004806] (76)
Oligodendroglioma [MESH:D009837] (241)
Glioblastoma [MESH:D005909] (2554)
Pheochromocytoma [MESH:D010673] (275)
C06. Digestive System Diseases
C06. Digestive System Diseases
Hirschsprung Disease [MESH:D006627] (361)
Intestinal Perforation [MESH:D007416] (471)
Hirschsprung Disease [MESH:D006627] (361)
C07. Stomatognathic Diseases
C07. Stomatognathic Diseases
Xerostomia [MESH:D014987] (98)
C08. Respiratory Tract Diseases
C08. Respiratory Tract Diseases
Hypertension, Pulmonary [MESH:D006976] (2000)
Congenital central hypoventilation syndrome [MESH:C536209] (341)
Congenital central hypoventilation syndrome [MESH:C536209] (341)
C10. Nervous System Diseases
C10. Nervous System Diseases
Not Fully Specified [NFS] (4027)
Trauma, Nervous System [MESH:D020196] (3997)
Huntington Disease [MESH:D006816] (540)
Parkinson Disease, Secondary [MESH:D010302] (327)
Parkinsonism-Dystonia, Infantile [MESH:C567730] (119)
Huntington Disease [MESH:D006816] (540)
Seizures [MESH:D012640] (4502)
Status Epilepticus [MESH:D013226] (4014)
Tic Disorders [MESH:D013981] (256)
Dyskinesia, Drug-Induced [MESH:D004409] (1389)
Huntington Disease [MESH:D006816] (540)
Parkinsonism-Dystonia, Infantile [MESH:C567730] (119)
Parkinson Disease, Secondary [MESH:D010302] (327)
Parkinsonism-Dystonia, Infantile [MESH:C567730] (119)
Huntington Disease [MESH:D006816] (540)
Parkinsonism-Dystonia, Infantile [MESH:C567730] (119)
Pain [MESH:D010146] (3875)
Seizures [MESH:D012640] (4514)
Hyperkinesis [MESH:D006948] (1799)
Memory Disorders [MESH:D008569] (3233)
Dizziness [MESH:D004244] (289)
Hyperalgesia [MESH:D006930] (3929)
Dyskinesia, Drug-Induced [MESH:D004409] (1389)
Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)
Cataplexy [MESH:D002385] (20)
Congenital central hypoventilation syndrome [MESH:C536209] (341)
C11. Eye Diseases
C11. Eye Diseases
Retinal Degeneration [MESH:D012162] (2386)
C12. Male Urogenital Diseases
C12. Male Urogenital Diseases
Not Fully Specified [NFS] (10)
Testicular Diseases [MESH:D013733] (451)
Erectile Dysfunction [MESH:D007172] (1791)
Urinary Retention [MESH:D016055] (411)
C13. Female Urogenital Diseases and Pregnancy Complications
C13. Female Urogenital Diseases and Pregnancy Complications
Urinary Retention [MESH:D016055] (411)
C14. Cardiovascular Diseases
C14. Cardiovascular Diseases
Cardiomyopathies [MESH:D009202] (5331)
Aortic Valve Insufficiency [MESH:D001022] (1002)
Mitral Valve Insufficiency [MESH:D008944] (35)
Hypertension [MESH:D006973] (5655)
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Hirschsprung Disease [MESH:D006627] (361)
Huntington Disease [MESH:D006816] (540)
C18. Nutritional and Metabolic Diseases
C18. Nutritional and Metabolic Diseases
Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
Insulin Resistance [MESH:D007333] (3511)
Obesity [MESH:D009765] (4462)
C19. Endocrine System Diseases
C19. Endocrine System Diseases
Diabetes Mellitus, Type 1 [MESH:D003922] (1897)
Testicular Diseases [MESH:D013733] (777)
C20. Immune System Diseases
C20. Immune System Diseases
Diabetes Mellitus, Type 1 [MESH:D003922] (1893)
C23. Pathological Conditions, Signs and Symptoms
C23. Pathological Conditions, Signs and Symptoms
Ventricular Remodeling [MESH:D020257] (686)
Nerve Degeneration [MESH:D009410] (4061)
Micronuclei, Chromosome-Defective [MESH:D048629] (1013)
Sudden Infant Death [MESH:D013398] (268)
Pain [MESH:D010146] (4511)
Fever [MESH:D005334] (2856)
Hypothermia [MESH:D007035] (2075)
Obesity [MESH:D009765] (4454)
Pain [MESH:D010146] (3869)
Seizures [MESH:D012640] (4502)
Hyperkinesis [MESH:D006948] (1799)
Memory Disorders [MESH:D008569] (3233)
Dizziness [MESH:D004244] (289)
Hyperalgesia [MESH:D006930] (3929)
Nausea [MESH:D009325] (2300)
Anoxia [MESH:D000860] (1698)
Congenital central hypoventilation syndrome [MESH:C536209] (341)
Dysuria [MESH:D053159] (29)
C25. Chemically-Induced Disorders
C25. Chemically-Induced Disorders
Dyskinesia, Drug-Induced [MESH:D004409] (1389)
Psychoses, Substance-Induced [MESH:D011605] (2053)
Dyskinesia, Drug-Induced [MESH:D004409] (1389)
Amphetamine-Related Disorders [MESH:D019969] (2858)
Cocaine-Related Disorders [MESH:D019970] (3054)
Psychoses, Substance-Induced [MESH:D011605] (2052)
Substance Withdrawal Syndrome [MESH:D013375] (2956)
Alcoholism [MESH:D000437] (1519)
Morphine Dependence [MESH:D009021] (855)
C26. Wounds and Injuries
C26. Wounds and Injuries
Trauma, Nervous System [MESH:D020196] (3535)
Radiation Injuries, Experimental [MESH:D011833] (2662)
D03. Heterocyclic Compounds
D03. Heterocyclic Compounds
Mazindol [MESH:D008454] (4)
F. Psychiatry and Psychology
F. Psychiatry and Psychology
Major Affective Disorder 1 [MESH:C565111] (237)