MeSH Treeview
Query OMIM entry list
590040
MTTH
TRANSFER RNA, MITOCHONDRIAL, HISTIDINE
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Digestive System Diseases
Liver Diseases
Fatty Liver
Reye Syndrome
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
MERRF Syndrome
Mitochondrial Encephalomyopathies
Reye Syndrome
Brain Edema
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
Dyskinesias
Ataxia
Pain
Headache
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinitis Pigmentosa
Lens Diseases
Cataract
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Male Urogenital Diseases
Genital Diseases, Male
Testicular Diseases
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
MERRF Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
MERRF Syndrome
Mitochondrial Encephalomyopathies
Reye Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
MERRF Syndrome
Mitochondrial Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Optic Atrophy, Hereditary, Leber
Endocrine System Diseases
Gonadal Disorders
Hypogonadism
Testicular Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Pain
Headache
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Pain
Headache
Database Center for Life Science
