MeSH Treeview
Query OMIM entry list
117210
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SPINOCEREBELLAR ATAXIA, 16q22-LINKED
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Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Dementia
Spinal Cord Diseases
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Optic Nerve Diseases
Optic Atrophy
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Gait Ataxia
Gait Disorders, Neurologic
Gait Ataxia
Paralysis
Ophthalmoplegia
Sensation Disorders
Hearing Disorders
Hearing Loss
Eye Diseases
Ocular Motility Disorders
Ophthalmoplegia
Optic Nerve Diseases
Optic Atrophy
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Gait Ataxia
Gait Disorders, Neurologic
Gait Ataxia
Paralysis
Ophthalmoplegia
Sensation Disorders
Hearing Disorders
Hearing Loss
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