190291
|
|
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Mitochondrially encoded tRNA arginine |
MTTR |
Curated: N/A
Unreviewed: Amyloidosis, Mitochondrial encephalomyopathy
|
190292
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
190293
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
190294
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
190295
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
190296
|
|
|
Mitochondrially encoded tRNA serine 1 (UCN) |
MTTS1 |
Curated: N/A
Unreviewed: Addison`s Disease, Anemia, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Ataxia, Attention Deficit Hyperactivity Disorder, Autism, Cataract, Central Visual Impairment, Cerebral cortical atrophy, Classical Hodgkin lymphoma, Cognition disorder, Congestive Heart Failure, Cytochrome-C Oxidase Deficiency, Deafness, Deafness, Nonsyndromic Sensorineural, Mitochondrial, Dementia, Developmental Delay, Developmental regression, Diabetes Mellitus, Dwarfism, Dysarthria, Epilepsy, Epileptic encephalopathy, Fanconi syndrome, Gastroparesis, Hallucinations, Hearing Loss, Heart Block, Hematomas, Hemianopsia, High palate, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired Cognition, Intestinal Obstruction, Left Ventricular Hypertrophy, Leukoencephalopathy, Malabsorption Syndrome, Malformation of cortical development, MELAS Syndrome, Mental Depression, Mental retardation, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Microcephaly, Migraine, Mitochondrial disease, Mitochondrial myopathy, Motor delay, Movement Disorders, Multiple Lipomata, Myoclonic Seizures, Myopathy, Nephrotic Syndrome, Nonsyndromic Deafness, Nyctalopia, Optic Atrophy, Palmoplantar keratoderma, Palmoplantar Keratoderma with Deafness, Pancreatitis, Phosphate Diabetes, Progressive External Ophthalmoplegia, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Renal Tubular Disorder, Retinitis Pigmentosa, Seizure, Sensorineural hearing loss, Sinus Thrombosis, Intracranial, Thyroiditis, Tremor, Wolff-Parkinson-White Syndrome
|
190297
|
|
|
Mitochondrially encoded tRNA serine 2 (AGU/C) |
MTTS2 |
Curated: N/A
Unreviewed: Addison`s Disease, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Astigmatism, Attention Deficit Hyperactivity Disorder, Autism, Cataract, Central Visual Impairment, Cerebral cortical atrophy, Congestive Heart Failure, Dementia, Developmental regression, Diabetes Mellitus, Dwarfism, Dysarthria, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing Loss, Heart Block, Hematomas, Hemianopsia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired Cognition, Intestinal Obstruction, Left Ventricular Hypertrophy, Malabsorption Syndrome, Malformation of cortical development, MELAS Syndrome, Mental Depression, MERRF Syndrome, MERRF/MELAS OVERLAP SYNDROME, Microcephaly, Migraine, Mitochondrial disease, Mitochondrial myopathy, Mitochondrial Respiratory Chain Deficiencies, Movement Disorders, Multiple Lipomata, Myoclonic Seizures, Myopathy, Nephrotic Syndrome, Nyctalopia, Optic Atrophy, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Retinal degeneration, Schizophrenia, Seizure, Sensorineural hearing loss, Thyroiditis, Usher Syndrome, Wolff-Parkinson-White Syndrome
|
190298
|
|
|
Mitochondrially encoded tRNA threonine |
MTTT |
Curated: N/A
Unreviewed: Cardiomyopathy, Cerebral cortical atrophy, Congenital alveolar dysplasia, Congenital Chromosomal Disease, Congestive Heart Failure, Diabetes Mellitus, Diabetic Nephropathy, Heart Failure, Henoch-Schonlein Nephritis, Kidney Disease, MERRF Syndrome, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial myopathy, Myoclonic epilepsy with ragged red fibers, Myopathy, Ovarian neoplasm, Parkinson Disease, Progressive External Ophthalmoplegia, Renal Insufficiency, Secondary Physiologic Amenorrhea
|
190299
|
|
|
- |
- |
Curated: N/A
Unreviewed: Cardiomyopathy, Cerebral cortical atrophy, Congenital alveolar dysplasia, Congenital Chromosomal Disease, Congestive Heart Failure, Diabetes Mellitus, Diabetic Nephropathy, Heart Failure, Henoch-Schonlein Nephritis, Kidney Disease, MERRF Syndrome, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial myopathy, Myoclonic epilepsy with ragged red fibers, Myopathy, Ovarian neoplasm, Parkinson Disease, Progressive External Ophthalmoplegia, Renal Insufficiency, Secondary Physiologic Amenorrhea
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190300
|
|
|
- |
- |
Curated: N/A
Unreviewed: Cardiomyopathy, Cerebral cortical atrophy, Congenital alveolar dysplasia, Congenital Chromosomal Disease, Congestive Heart Failure, Diabetes Mellitus, Diabetic Nephropathy, Heart Failure, Henoch-Schonlein Nephritis, Kidney Disease, MERRF Syndrome, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial myopathy, Myoclonic epilepsy with ragged red fibers, Myopathy, Ovarian neoplasm, Parkinson Disease, Progressive External Ophthalmoplegia, Renal Insufficiency, Secondary Physiologic Amenorrhea
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