Genes?

Curated: N/A

Unreviewed: Aicardi goutieres syndrome, Alzheimer disease, Amyotrophic lateral sclerosis, Ataxia, Ataxia telangiectasia, Atrophy, Autism, Autoimmune hepatitis, Basal ganglia disease, Bipolar disorder, Bone disease, Brain disease, Breast neoplasm, Brugada syndrome, Carcinogenesis, Cardiomyopathy, Cardiovascular abnormalities, Cartilage disease, Central nervous system disease, Cerebellar ataxia, Cerebral hemorrhage, Chondrosarcoma, Cognition disorder, Colorectal neoplasm, Coronary artery disease, Cyclic neutropenia, Cytochrome c oxidase deficiency, Deafness, Developmental disability, Diabetes mellitus, Diabetes mellitus, type 2, Dilated cardiomyopathy, Disorders of sex development, Dysautonomia, Epilepsy, Episodic ataxia, Esophageal squamous cell carcinoma, Facial dysmorphism syndrome, Galloway-mowat syndrome, Gastroesophageal reflux disease, Gastrointestinal hemorrhage, Glycogen storage disease, Growth disorder, Headache, Hearing loss, Heart disease, Huntington disease, Hypertension, Hypertrophic cardiomyopathy, Hyperuricemia, Hypoparathyroidism, Idiopathic pulmonary fibrosis, Intellectual developmental disorder, Kidney disease, Kidney failure, Lactic acidosis, Leber hereditary optic neuropathy, Left ventricular disease, Leigh syndrome, Leukemia, Lipoma, Liver failure, Lung neoplasms, Major depressive disorder, Medullary carcinoma, Melanoma, Melas syndrome, Mesothelioma, Migraine, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy, Mitochondrial myopathy, Mitochondrial myopathy with sideroblastic anemia, Multiple myeloma, Multiple sclerosis, Multiple system atrophy, Myelodysplastic syndrome, Myeloid leukemia, Myoclonic epilepsy, Myoclonic epilepsy with ragged red fibers, Myopia, Myositis, Myotonia congenita, Nasopharyngeal carcinoma, Nemaline myopathy, Neuroblastoma, Neurodegenerative disorder, Neuromuscular disease, Obesity, Ophthalmoplegia, Osteoarthritis, Pancreatic ductal carcinoma, Pancreatic neoplasm, Pancreatitis, Papillary thyroid cancer, Parkinson disease, Pituitary dwarfism, Progressive external ophthalmoplegia, Promyelocytic leukemia, Prostatic neoplasm, Proteinuria, Retinitis pigmentosa, Rheumatoid arthritis, Schilder disease, Squamous cell carcinoma, Stomach neoplasms, Stroke, Testicular germ cell tumor, Thyroid cancer, Triple negative breast cancer, Varicose veins, Visceral neuropathy, Visual disorder, Werner syndrome, Xeroderma pigmentosum

Curated: N/A

Unreviewed: Addison`s Disease, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention Deficit Hyperactivity Disorder, Autism, Cataract, Cerebral cortical atrophy, Congestive Heart Failure, Developmental regression, Diabetes Mellitus, Dwarfism, Dysarthria, Gastroparesis, Hallucinations, Hearing Loss, Heart Block, Hematomas, Hemianopsia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired Cognition, Intestinal Obstruction, Keratoconus, Malabsorption Syndrome, Malformation of cortical development, MELAS Syndrome, Mental Depression, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Microcephaly, Migraine, Mitochondrial myopathy, Movement Disorders, Multiple Lipomata, Myoclonic Seizures, Myopathy, Nephrotic Syndrome, Nyctalopia, Optic Atrophy, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Seizure, Thyroiditis, Wolff-Parkinson-White Syndrome

Curated: N/A

Unreviewed: Addison`s Disease, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention Deficit Hyperactivity Disorder, Autism, Cataract, Cerebral cortical atrophy, Congestive Heart Failure, Developmental regression, Diabetes Mellitus, Dwarfism, Dysarthria, Gastroparesis, Hallucinations, Hearing Loss, Heart Block, Hematomas, Hemianopsia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired Cognition, Intestinal Obstruction, Keratoconus, Malabsorption Syndrome, Malformation of cortical development, MELAS Syndrome, Mental Depression, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Microcephaly, Migraine, Mitochondrial myopathy, Movement Disorders, Multiple Lipomata, Myoclonic Seizures, Myopathy, Nephrotic Syndrome, Nyctalopia, Optic Atrophy, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Seizure, Thyroiditis, Wolff-Parkinson-White Syndrome

Curated: N/A

Unreviewed: Addison`s Disease, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention Deficit Hyperactivity Disorder, Autism, Cataract, Cerebral cortical atrophy, Congestive Heart Failure, Developmental regression, Diabetes Mellitus, Dwarfism, Dysarthria, Gastroparesis, Hallucinations, Hearing Loss, Heart Block, Hematomas, Hemianopsia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired Cognition, Intestinal Obstruction, Keratoconus, Malabsorption Syndrome, Malformation of cortical development, MELAS Syndrome, Mental Depression, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Microcephaly, Migraine, Mitochondrial myopathy, Movement Disorders, Multiple Lipomata, Myoclonic Seizures, Myopathy, Nephrotic Syndrome, Nyctalopia, Optic Atrophy, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Seizure, Thyroiditis, Wolff-Parkinson-White Syndrome

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: 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