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602125
COX10
CYTOCHROME c OXIDASE ASSEMBLY PROTEIN COX10
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Cytochrome-c Oxidase Deficiency
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Leigh Disease
Database Center for Life Science