MeSH Treeview
Query OMIM entry list
182138
SLC6A4
SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, SEROTONIN), MEMBER 4
→
High-scoring List
Virus Diseases
DNA Virus Infections
Herpesviridae Infections
Epstein-Barr Virus Infections
Burkitt Lymphoma
Tumor Virus Infections
Epstein-Barr Virus Infections
Burkitt Lymphoma
Parasitic Diseases
Helminthiasis
Nematode Infections
Adenophorea Infections
Enoplida Infections
Trichinellosis
Neoplasms
Neoplasms by Histologic Type
Lymphoma
Lymphoma, Non-Hodgkin
Burkitt Lymphoma
Lymphoma, B-Cell
Burkitt Lymphoma
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Glioma
Trophoblastic Neoplasms
Choriocarcinoma
Gestational Trophoblastic Disease
Choriocarcinoma
Neoplasms, Glandular and Epithelial
Carcinoma
Adenocarcinoma
Choriocarcinoma
Neoplasms, Neuroepithelial
Glioma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Glioma
Neoplasms by Site
Urogenital Neoplasms
Genital Neoplasms, Female
Uterine Neoplasms
Neoplasms, Experimental
Tumor Virus Infections
Epstein-Barr Virus Infections
Burkitt Lymphoma
Pregnancy Complications, Neoplastic
Trophoblastic Neoplasms
Gestational Trophoblastic Disease
Choriocarcinoma
Tumor Virus Infections
Epstein-Barr Virus Infections
Burkitt Lymphoma
Musculoskeletal Diseases
Muscular Diseases
Fibromyalgia
Rheumatic Diseases
Fibromyalgia
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Colonic Diseases
Colonic Diseases, Functional
Irritable Bowel Syndrome
Respiratory Tract Diseases
Lung Diseases
Hypertension, Pulmonary
Lung Diseases, Obstructive
Pulmonary Disease, Chronic Obstructive
Nervous System Diseases
Autonomic Nervous System Diseases
Primary Dysautonomias
Multiple System Atrophy
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Multiple System Atrophy
Parkinsonian Disorders
Parkinson Disease
Parkinson Disease, Secondary
MPTP Poisoning
Tourette Syndrome
Cerebrovascular Disorders
Stroke
Dementia
Alzheimer Disease
Epilepsy
Epilepsy, Generalized
Epilepsy, Tonic-Clonic
Seizures
Headache Disorders
Headache Disorders, Primary
Migraine Disorders
Migraine with Aura
Movement Disorders
Multiple System Atrophy
Parkinsonian Disorders
Parkinson Disease
Parkinson Disease, Secondary
MPTP Poisoning
Tic Disorders
Tourette Syndrome
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Rett Syndrome
Tourette Syndrome
Multiple System Atrophy
Parkinson Disease
Tauopathies
Alzheimer Disease
Neurologic Manifestations
Dyskinesias
Hypokinesia
Neurobehavioral Manifestations
Memory Disorders
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Rett Syndrome
Seizures
Sensation Disorders
Somatosensory Disorders
Neuromuscular Diseases
Muscular Diseases
Fibromyalgia
Neurotoxicity Syndromes
MPTP Poisoning
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Genital Diseases, Female
Uterine Diseases
Uterine Neoplasms
Urogenital Neoplasms
Genital Neoplasms, Female
Uterine Neoplasms
Pregnancy Complications
Hypertension, Pregnancy-Induced
Pre-Eclampsia
Pregnancy Complications, Neoplastic
Trophoblastic Neoplasms
Gestational Trophoblastic Disease
Choriocarcinoma
Prenatal Injuries
Prenatal Exposure Delayed Effects
Puerperal Disorders
Depression, Postpartum
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Hypertrophy, Right Ventricular
Myocardial Ischemia
Myocardial Infarction
Vascular Diseases
Cerebrovascular Disorders
Stroke
Hypertension
Myocardial Ischemia
Myocardial Infarction
Hemic and Lymphatic Diseases
Lymphatic Diseases
Lymphoproliferative Disorders
Lymphoma
Lymphoma, Non-Hodgkin
Burkitt Lymphoma
Lymphoma, B-Cell
Burkitt Lymphoma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Rett Syndrome
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Fragile X Syndrome
Rett Syndrome
Rett Syndrome
Tourette Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hypercholesterolemia
Immune System Diseases
Hypersensitivity
Immunoproliferative Disorders
Lymphoproliferative Disorders
Lymphoma
Lymphoma, Non-Hodgkin
Burkitt Lymphoma
Lymphoma, B-Cell
Burkitt Lymphoma
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Hypertrophy
Cardiomegaly
Hypertrophy, Right Ventricular
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Death
Asphyxia
Cadaver
Postmortem Changes
Death, Sudden
Sudden Infant Death
Disease Attributes
Acute Disease
Chronic Disease
Disease Susceptibility
Genetic Predisposition to Disease
Hyperplasia
Nerve Degeneration
Wallerian Degeneration
Signs and Symptoms
Body Weight
Neurologic Manifestations
Dyskinesias
Hypokinesia
Neurobehavioral Manifestations
Memory Disorders
Seizures
Sensation Disorders
Somatosensory Disorders
Signs and Symptoms, Digestive
Hyperphagia
Bulimia
Signs and Symptoms, Respiratory
Anoxia
Substance-Related Disorders
Alcohol-Related Disorders
Alcoholism
Amphetamine-Related Disorders
Cocaine-Related Disorders
Opioid-Related Disorders
Heroin Dependence
Poisoning
Drug Toxicity
Serotonin Syndrome
Neurotoxicity Syndromes
MPTP Poisoning
Wounds and Injuries
Asphyxia
Database Center for Life Science