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Query OMIM entry list
204100
LCA2
LEBER CONGENITAL AMAUROSIS, TYPE II
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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
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinal Diseases
Retinal Degeneration
Vision Disorders
Blindness
Night Blindness
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Diseases, Cystic
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Diseases, Cystic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Blindness
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