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605020
VSX1
VISUAL SYSTEM HOMEOBOX GENE 1, ZEBRAFISH, HOMOLOG OF
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Otorhinolaryngologic Diseases
Ear Diseases
Retrocochlear Diseases
Auditory Diseases, Central
Auditory Perceptual Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Auditory Diseases, Central
Auditory Perceptual Disorders
Hypothalamic Diseases
Pituitary Diseases
Empty Sella Syndrome
Neurologic Manifestations
Neurobehavioral Manifestations
Perceptual Disorders
Auditory Perceptual Disorders
Eye Diseases
Corneal Diseases
Corneal Dystrophies, Hereditary
Fuchs' Endothelial Dystrophy
Keratoconus
Eye Abnormalities
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Fuchs' Endothelial Dystrophy
Retinal Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Fuchs' Endothelial Dystrophy
Endocrine System Diseases
Pituitary Diseases
Empty Sella Syndrome
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Perceptual Disorders
Auditory Perceptual Disorders
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