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300556
ATP6AP2
ATPase, H+ TRANSPORTING, LYSOSOMAL, ACCESSORY PROTEIN 2
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Musculoskeletal Diseases
Bone Diseases
Spinal Diseases
Spinal Curvatures
Scoliosis
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Neurologic Manifestations
Gait Disorders, Neurologic
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Sensation Disorders
Vision Disorders
Color Vision Defects
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Color Vision Defects
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Gait Disorders, Neurologic
Neurobehavioral Manifestations
Intellectual Disability
Sensation Disorders
Vision Disorders
Color Vision Defects
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