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608507
MFN2
MITOFUSIN 2
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Musculoskeletal Diseases
Muscular Diseases
Muscle Weakness
Nervous System Diseases
Central Nervous System Diseases
Movement Disorders
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
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
Optic Atrophies, Hereditary
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Abortion, Spontaneous
Embryo Loss
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Optic Atrophies, Hereditary
Nutritional and Metabolic Diseases
Nutrition Disorders
Overnutrition
Obesity
Obesity, Morbid
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Death
Embryo Loss
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Muscle Weakness
Signs and Symptoms
Body Weight
Overweight
Obesity
Obesity, Morbid
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
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