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Query OMIM entry list
180069
RPE65
RETINAL PIGMENT EPITHELIUM-SPECIFIC PROTEIN, 65-KD
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Nervous System Diseases
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Blindness
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinitis Pigmentosa
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Blindness
Night Blindness
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Optic Atrophy, Hereditary, Leber
Animal Diseases
Disease Models, Animal
Dog Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Nondisjunction, Genetic
Uniparental Disomy
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Blindness
Database Center for Life Science
