MeSH Treeview
Query OMIM entry list
607426
-
COENZYME Q10 DEFICIENCY
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Muscle Weakness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Mitochondrial Encephalomyopathies
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Degenerations
Epilepsy
Seizures
Spinal Cord Diseases
Spinocerebellar Degenerations
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Seizures
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Eye Diseases
Retinal Diseases
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Pregnancy Complications
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Protein Disorders
Hypoproteinemia
Hypoalbuminemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Lipid Metabolism, Inborn Errors
Hyperlipoproteinemia Type II
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Mitochondrial Encephalomyopathies
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hyperlipoproteinemias
Hyperlipoproteinemia Type II
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Lipid Metabolism, Inborn Errors
Hyperlipoproteinemia Type II
Mitochondrial Diseases
Leigh Disease
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Endocrine System Diseases
Gonadal Disorders
Hypogonadism
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Disease Attributes
Disease Progression
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Seizures
Database Center for Life Science