MeSH Treeview
Query OMIM entry list
310500
CSNB1A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A
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Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Nystagmus, Congenital
Strabismus
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Eye Diseases
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Retinitis Pigmentosa
Ocular Motility Disorders
Nystagmus, Pathologic
Nystagmus, Congenital
Strabismus
Refractive Errors
Hyperopia
Myopia
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Night Blindness
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Muscular Dystrophies
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Infant, Newborn, Diseases
Nystagmus, Congenital
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Ocular
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Vision Disorders
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