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516005
MTND5
COMPLEX I, SUBUNIT ND5
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Metabolic
Mucolipidoses
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
MELAS Syndrome
MERRF Syndrome
Mitochondrial Encephalomyopathies
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
MERRF Syndrome
Seizures
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Neurologic Manifestations
Gait Disorders, Neurologic
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Aphasia
Confusion
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Vision Disorders
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Vision Disorders
Cardiovascular Diseases
Heart Diseases
Arrhythmias, Cardiac
Pre-Excitation Syndromes
Wolff-Parkinson-White Syndrome
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Cardiovascular Abnormalities
Heart Defects, Congenital
Wolff-Parkinson-White Syndrome
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
MELAS Syndrome
MERRF Syndrome
Carbohydrate Metabolism, Inborn Errors
Mucolipidoses
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
MELAS Syndrome
MERRF Syndrome
Mitochondrial Encephalomyopathies
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
MELAS Syndrome
MERRF Syndrome
Carbohydrate Metabolism, Inborn Errors
Mucolipidoses
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Mucolipidoses
Mitochondrial Diseases
Leigh Disease
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Optic Atrophy, Hereditary, Leber
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Gait Disorders, Neurologic
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Aphasia
Confusion
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Vision Disorders
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