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516020
MTCYB
CYTOCHROME b OF COMPLEX III
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Neoplasms
Neoplasms by Site
Digestive System Neoplasms
Gastrointestinal Neoplasms
Intestinal Neoplasms
Colorectal Neoplasms
Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Rhabdomyolysis
Myoglobinuria
Digestive System Diseases
Digestive System Neoplasms
Gastrointestinal Neoplasms
Intestinal Neoplasms
Colorectal Neoplasms
Gastrointestinal Diseases
Gastrointestinal Neoplasms
Intestinal Neoplasms
Colorectal Neoplasms
Intestinal Diseases
Colonic Diseases
Colorectal Neoplasms
Intestinal Neoplasms
Colorectal Neoplasms
Rectal Diseases
Colorectal Neoplasms
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Hearing Loss, Bilateral
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Parkinson Disease, Secondary
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
Mitochondrial Encephalomyopathies
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Epilepsy
Movement Disorders
Parkinsonian Disorders
Parkinson Disease, Secondary
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Nervous System Malformations
Septo-Optic Dysplasia
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Pain
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Bilateral
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Retinitis Pigmentosa
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Septo-Optic Dysplasia
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
Mitochondrial Encephalomyopathies
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
Mitochondrial Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Pain
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Bilateral
Pain
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