Genes?

Curated: N/A

Unreviewed: Cardiomyopathy, Deafness, Nonsyndromic Sensorineural, Mitochondrial, Hearing Loss, Hypercholesterolemia, Hypertension, Hypertrophic cardiomyopathy, MELAS Syndrome, MERRF Syndrome, Mitochondrial Cardiomyopathy, Mitochondrial Hypomagnesemia, Hypertension, And Hypercholesterolemia, Myoclonic Seizures, Myopathy, Progressive External Ophthalmoplegia

Curated: N/A

Unreviewed: Cardiomyopathy, Deafness, Nonsyndromic Sensorineural, Mitochondrial, Hearing Loss, Hypercholesterolemia, Hypertension, Hypertrophic cardiomyopathy, MELAS Syndrome, MERRF Syndrome, Mitochondrial Cardiomyopathy, Mitochondrial Hypomagnesemia, Hypertension, And Hypercholesterolemia, Myoclonic Seizures, Myopathy, Progressive External Ophthalmoplegia

Curated: N/A

Unreviewed: Age-related macular degeneration, Cardiomyopathy, Cataract, Central Visual Impairment, Coenzyme q10 deficiency, Congestive Heart Failure, Cytochrome c oxidase deficiency, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes and Hearing Loss, Diabetes Mellitus, Dwarfism, Dyskinetic Syndrome, Dysphagia, Epilepsy, Epileptic encephalopathy, External Ophthalmoplegia, Febrile seizures, Hearing Loss, Hemianopsia, Hereditary Leber Optic Atrophy, Hypertension, Hypertrophic cardiomyopathy, Hypotonic seizures, Impaired Cognition, Lactic acidosis, Left Ventricular Hypertrophy, Leigh Syndrome, Liver failure, Malabsorption Syndrome, Maternally Inherited Leigh Syndrome, MELAS Syndrome, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Migraine, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial DNA Depletion Syndrome, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy, Mitochondrial myopathy, Movement Disorders, Multiple Lipomata, Myoclonic Epilepsy, Myoclonic epilepsy with ragged red fibers, Myoclonic Seizures, Myopathy, Nervous System Diseases, Nystagmus, Optic Atrophy, Parkinson Disease, Progressive External Ophthalmoplegia, Ptosis, Renal Glomerular Disease, Renal Insufficiency, Retinal Diseases, Retinitis Pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Stroke, West Syndrome, Wolff-Parkinson-White Syndrome

Curated: N/A

Unreviewed: Age-related macular degeneration, Cardiomyopathy, Cataract, Central Visual Impairment, Coenzyme q10 deficiency, Congestive Heart Failure, Cytochrome c oxidase deficiency, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes and Hearing Loss, Diabetes Mellitus, Dwarfism, Dyskinetic Syndrome, Dysphagia, Epilepsy, Epileptic encephalopathy, External Ophthalmoplegia, Febrile seizures, Hearing Loss, Hemianopsia, Hereditary Leber Optic Atrophy, Hypertension, Hypertrophic cardiomyopathy, Hypotonic seizures, Impaired Cognition, Lactic acidosis, Left Ventricular Hypertrophy, Leigh Syndrome, Liver failure, Malabsorption Syndrome, Maternally Inherited Leigh Syndrome, MELAS Syndrome, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Migraine, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial DNA Depletion Syndrome, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy, Mitochondrial myopathy, Movement Disorders, Multiple Lipomata, Myoclonic Epilepsy, Myoclonic epilepsy with ragged red fibers, Myoclonic Seizures, Myopathy, Nervous System Diseases, Nystagmus, Optic Atrophy, Parkinson Disease, Progressive External Ophthalmoplegia, Ptosis, Renal Glomerular Disease, Renal Insufficiency, Retinal Diseases, Retinitis Pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Stroke, West Syndrome, Wolff-Parkinson-White Syndrome

Curated: N/A

Unreviewed: Age-related macular degeneration, Cardiomyopathy, Cataract, Central Visual Impairment, Coenzyme q10 deficiency, Congestive Heart Failure, Cytochrome c oxidase deficiency, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes and Hearing Loss, Diabetes Mellitus, Dwarfism, Dyskinetic Syndrome, Dysphagia, Epilepsy, Epileptic encephalopathy, External Ophthalmoplegia, Febrile seizures, Hearing Loss, Hemianopsia, Hereditary Leber Optic Atrophy, Hypertension, Hypertrophic cardiomyopathy, Hypotonic seizures, Impaired Cognition, Lactic acidosis, Left Ventricular Hypertrophy, Leigh Syndrome, Liver failure, Malabsorption Syndrome, Maternally Inherited Leigh Syndrome, MELAS Syndrome, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Migraine, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial DNA Depletion Syndrome, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy, Mitochondrial myopathy, Movement Disorders, Multiple Lipomata, Myoclonic Epilepsy, Myoclonic epilepsy with ragged red fibers, Myoclonic Seizures, Myopathy, Nervous System Diseases, Nystagmus, Optic Atrophy, Parkinson Disease, Progressive External Ophthalmoplegia, Ptosis, Renal Glomerular Disease, Renal Insufficiency, Retinal Diseases, Retinitis Pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Stroke, West Syndrome, Wolff-Parkinson-White Syndrome

Curated: N/A

Unreviewed: N/A

Curated: N/A

Unreviewed: N/A

Curated: N/A

Unreviewed: N/A

Curated: N/A

Unreviewed: N/A

Curated: N/A

Unreviewed: Addison`s Disease, Age-related macular degeneration, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arteriosclerosis, Arthrogryposis multiplex congenita, Atherosclerosis, Attention Deficit Hyperactivity Disorder, Autism, Brain disease, Breast neoplasm, Cardiac arrhythmias, Cardiomyopathy, Cardiovascular Diseases, Cataract, Central Visual Impairment, Cerebral cortical atrophy, Chorea, Cognition disorder, Complete Atrioventricular Block, Congestive Heart Failure, Cyclical Vomiting Syndrome, Cytochrome-C Oxidase Deficiency, Deafness, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes, Diabetes and Hearing Loss, Diabetes Mellitus, Diabetes mellitus, type 2, Dwarfism, Dysarthria, Dyskinetic Syndrome, Dysphagia, Epidermolysa bullosa simplex and limb girdle muscular dystrophy, Epilepsy, Epileptic encephalopathy, External Ophthalmoplegia, Focal segmental glomerulosclerosis, Gastroparesis, Gestational diabetes, Glomerulosclerosis, Hallucinations, Hearing Loss, Heart Block, Heart disease, Hematomas, Hematuria, Hemianopsia, Hemiplegia/hemiparesis, Hyperkinesia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypertrophic Cardiomyopathy And Renal Tubular Disease, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired Cognition, Intellectual developmental disorder, Intestinal Obstruction, Intestinal Pseudoobstruction, Kearns Sayre Syndrome, Kidney disease, Lactic acidosis, Left Ventricular Hypertrophy, Leigh Syndrome, Liver failure, Malabsorption Syndrome, Malformation of cortical development, Maternally Inherited Leigh Syndrome, MELAS Syndrome, Mental Depression, Mental retardation, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Microcephaly, Migraine, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy, Mitochondrial myopathy, Movement Disorders, Multiple Lipomata, Multiple Sclerosis, Myelodysplastic Syndrome, Myoclonic epilepsy, Myoclonic epilepsy with ragged red fibers, Myoclonic Seizures, Myopathy, Myositis, Nephrotic Syndrome, Nyctalopia, Nystagmus, Optic Atrophy, Optic neuropathy, Pancreatitis, Parkinson disease, Progressive External Ophthalmoplegia, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Retinal Diseases, Retinitis Pigmentosa, Rod-cone dystrophy, Seizure, Seizures, Sensorimotor neuropathy, Sensorineural hearing loss, Sexual Dysfunction, Status epilepticus, Stroke, Thyroiditis, West Syndrome, Wolff-Parkinson-White Syndrome