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300630
MRX59
MENTAL RETARDATION, X-LINKED 59
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Hydrocephalus
Intracranial Hypertension
Hydrocephalus
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Optic Atrophies, Hereditary
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Calcinosis
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Database Center for Life Science
