|
321
|
|
|
Mitochondrially encoded tRNA lysine |
MTTK |
Cardiomyopathy, Cataract, Central visual impairment, Congestive heart failure, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes and hearing loss, Diabetes mellitus, Dwarfism, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, External ophthalmoplegia, Febrile seizures, Hearing loss, Hemianopsia, Hypertension, Hypertrophic cardiomyopathy, Impaired cognition, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Age-related macular degeneration, Malabsorption syndrome, Maternally inherited leigh syndrome, Melas syndrome, Merrf syndrome, Merrf/melas overlap syndrome, Migraine, Mitochondrial diseases, Mitochondrial dna depletion syndrome, Mitochondrial myopathy, Movement disorders, Multiple lipomata, Myoclonic seizures, Myopathy, Nervous system diseases, Nystagmus, Optic atrophy, Parkinson disease, Progressive external ophthalmoplegia, Renal glomerular disease, Renal insufficiency, Retinal diseases, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, West syndrome, Wolff-parkinson-white syndromeView all (37 more) |
|
322
|
|
|
Mitochondrially encoded tRNA leucine 1 (UUA/G) |
MTTL1 |
Addison`s disease, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cardiomyopathy, Cataract, Central visual impairment, Cerebral cortical atrophy, Complete atrioventricular block, Congestive heart failure, Cyclical vomiting syndrome, Cytochrome-c oxidase deficiency, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes and hearing loss, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, External ophthalmoplegia, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hemiplegia/hemiparesis, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy and renal tubular disease, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Impaired cognition, Intestinal obstruction, Kearns sayre syndrome, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Age-related macular degeneration, 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 diseases, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Movement disorders, Multiple lipomata, Myelodysplastic syndrome, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nyctalopia, Nystagmus, Optic atrophy, Pancreatitis, Progressive external ophthalmoplegia, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinal diseases, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Stroke, Thyroiditis, West syndrome, Wolff-parkinson-white syndromeView all (74 more) |
|
323
|
|
|
Mitochondrially encoded tRNA leucine 2 (CUN) |
MTTL2 |
|
|
324
|
|
|
Mitochondrially encoded tRNA methionine |
MTTM |
|
|
325
|
|
|
Mitochondrially encoded tRNA asparagine |
MTTN |
Anemia, Cytochrome-c oxidase deficiency, Developmental delay, External ophthalmoplegia, Fanconi syndrome, Hearing loss, High palate, Hypertrophic cardiomyopathy, Hypothyroidism, Leukoencephalopathy, Melas syndrome, Mental depression, Mental retardation, Motor delay, Optic atrophy, Phosphate diabetes, Progressive external ophthalmoplegia, Ptosis, Renal tubular disorder, Retinitis pigmentosaView all (5 more) |
|
326
|
|
|
Mitochondrially encoded tRNA proline |
MTTP |
|
|
327
|
|
|
Mitochondrially encoded tRNA glutamine |
MTTQ |
Addison`s disease, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, 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, 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, Sensorineural hearing loss, Thyroiditis, Wolff-parkinson-white syndromeView all (45 more) |
|
328
|
|
|
Mitochondrially encoded tRNA arginine |
MTTR |
|
|
329
|
|
|
Mitochondrially encoded tRNA serine 1 (UCN) |
MTTS1 |
Addison`s disease, Anemia, Anorexia, Anxiety disorder, Aortic aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Cataract, Central visual impairment, Cerebral cortical atrophy, Congestive heart failure, Cytochrome-c oxidase deficiency, Deafness, Deafness, nonsyndromic sensorineural, mitochondrial, Dementia, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, 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 myopathy, Motor delay, Movement disorders, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nyctalopia, Optic atrophy, Palmoplantar keratoderma with deafness, Palmoplantar keratoderma, 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, Thyroiditis, Wolff-parkinson-white syndromeView all (62 more) |
|
330
|
|
|
Mitochondrially encoded tRNA serine 2 (AGU/C) |
MTTS2 |
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 myopathy, Movement disorders, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nyctalopia, Optic atrophy, Pancreatitis, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Schizophrenia, Seizure, Sensorineural hearing loss, Thyroiditis, Usher syndrome, Wolff-parkinson-white syndromeView all (49 more) |
