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Query OMIM entry list
600111
SLC1A3
SOLUTE CARRIER FAMILY 1 (GLIAL HIGH AFFINITY GLUTAMATE TRANSPORTER), MEMBER 3
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Lewy Body Disease
Parkinson Disease
Brain Edema
Cerebrovascular Disorders
Brain Ischemia
Brain Infarction
Cerebral Infarction
Dementia, Multi-Infarct
Dementia, Vascular
Dementia, Multi-Infarct
Stroke
Brain Infarction
Cerebral Infarction
Dementia, Multi-Infarct
Dementia
Alzheimer Disease
Dementia, Vascular
Dementia, Multi-Infarct
Lewy Body Disease
Epilepsy
Seizures
Movement Disorders
Parkinsonian Disorders
Lewy Body Disease
Parkinson Disease
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Lewy Body Disease
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Parkinson Disease
Tauopathies
Alzheimer Disease
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Neurologic Manifestations
Dyskinesias
Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypertonia
Paralysis
Hemiplegia
Seizures
Neuromuscular Diseases
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinal Diseases
Retinal Detachment
Cardiovascular Diseases
Vascular Diseases
Cerebrovascular Disorders
Brain Ischemia
Brain Infarction
Cerebral Infarction
Dementia, Multi-Infarct
Stroke
Brain Infarction
Cerebral Infarction
Dementia, Multi-Infarct
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Optic Atrophy, Hereditary, Leber
Proteostasis Deficiencies
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Chromosome Duplication
Trisomy
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Ischemia
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypertonia
Paralysis
Hemiplegia
Seizures
Signs and Symptoms, Respiratory
Hyperoxia
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