MeSH Treeview
Query OMIM entry list
176980
PRKCG
PROTEIN KINASE C, GAMMA
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Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Spinal Cord Diseases
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Nervous System Malformations
Neural Tube Defects
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Myotonic Dystrophy
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Neural Tube Defects
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Myotonic Dystrophy
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Muscular Dystrophies
Myotonic Dystrophy
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Translocation, Genetic
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
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