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603247
SLC27A2
SOLUTE CARRIER FAMILY 27 (FATTY ACID TRANSPORTER), MEMBER 2
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Adrenoleukodystrophy
Peroxisomal Disorders
Adrenoleukodystrophy
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Adrenoleukodystrophy
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Adrenoleukodystrophy
Demyelinating Diseases
Hereditary Central Nervous System Demyelinating Diseases
Adrenoleukodystrophy
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Adrenoleukodystrophy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Adrenoleukodystrophy
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Adrenoleukodystrophy
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Adrenoleukodystrophy
Peroxisomal Disorders
Adrenoleukodystrophy
Peroxisomal Disorders
Adrenoleukodystrophy
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Adrenoleukodystrophy
Peroxisomal Disorders
Adrenoleukodystrophy
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Adrenoleukodystrophy
Peroxisomal Disorders
Adrenoleukodystrophy
Peroxisomal Disorders
Adrenoleukodystrophy
Endocrine System Diseases
Adrenal Gland Diseases
Adrenal Insufficiency
Adrenoleukodystrophy
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