MeSH Treeview
Query OMIM entry list
300036
SLC6A8
SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, CREATINE), MEMBER 8
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Epilepsy
Seizures
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Neuromuscular Manifestations
Muscle Hypotonia
Seizures
Neuromuscular Diseases
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
Seizures
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