|
331
|
|
|
Mitochondrially encoded tRNA threonine |
MTTT |
Congenital alveolar dysplasia, Cardiomyopathy, Cerebral cortical atrophy, Merrf syndrome, Mitochondrial diseases, Mitochondrial myopathy, Myopathy, Ovarian neoplasm, Parkinson disease, Progressive external ophthalmoplegia, Renal insufficiency, Secondary physiologic amenorrhea |
|
332
|
|
|
Mitochondrially encoded tRNA valine |
MTTV |
Cardiomyopathy, Central visual impairment, Congestive heart failure, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes mellitus, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Hearing loss, Hemianopsia, Hypertension, Hypertrophic cardiomyopathy, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Maternally inherited leigh syndrome, Melas syndrome, Migraine, Mitochondrial myopathy, Myoclonic seizures, Myopathy, Nystagmus, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, West syndrome, Wolff-parkinson-white syndromeView all (17 more) |
|
333
|
|
|
Mitochondrially encoded tRNA tryptophan |
MTTW |
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, Congestive heart failure, Dementia, Demyelinating neuropathy, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Gastroparesis, Hallucinations, Hearing loss, Heart block, Hematomas, Hemianopsia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Intestinal obstruction, Left ventricular hypertrophy, Leigh syndrome, Liver failure, Luft disease, Macroglossia, Malabsorption syndrome, Malformation of cortical development, Maternally inherited leigh syndrome, Megaconial myopathies, Melas syndrome, Mental depression, Microcephaly, Migraine, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy, Mitochondrial myopathy, Motor delay, Multiple lipomata, Myoclonic seizures, Myopathy, Nephrotic syndrome, Nyctalopia, Nystagmus, Optic atrophy, Pancreatitis, Pleoconial myopathy, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensorineural hearing loss, Thyroiditis, West syndrome, Wolff-parkinson-white syndromeView all (61 more) |
|
334
|
|
|
Mitochondrially encoded tRNA tyrosine |
MTTY |
|
|
335
|
|
|
Tripartite motif containing 37 |
MUL, POB1, TEF3 |
Astigmatism, Congestive heart failure, Dolichocephaly, Dwarfism, Dysarthria, Fibrocartilaginous dysplasia of bone, Fibrocystic dysplasia of bone, Fibrous dysplasia, Frontal bossing, Hypodontia, Joubert syndrome, Macrocephaly, Microglossia, Mulibrey nanism, Nephroblastoma, Nevus, Pericardial constriction with growth failure, Retinitis pigmentosa, StrabismusView all (4 more) |
|
336
|
|
|
Tonsoku like, DNA repair protein |
IKBR, NFKBIL2, SEMDSP |
Acquired kyphoscoliosis, Capsular cataract, Cataract, Congenital kyphoscoliosis, Frontal bossing, Liver carcinoma, Macrocephaly, Malocclusion, Mesomelia, Osteopenia, Osteoporosis, Sclerocystic ovaries, Polycystic ovary syndrome, Rhizomelia, Scoliosis, Sponastrime dysplasia, Spondyloenchondrodysplasia, Spondyloepimetaphyseal dysplasiaView all (3 more) |
|
337
|
|
|
TBC1 domain family member 25 |
MG81, OATL1 |
|
|
338
|
|
|
TYMS opposite strand RNA |
C18orf56 |
|
|
339
|
|
|
TNF receptor superfamily member 11b |
OCIF, OPG, PDB5, TR1 |
Angioid streaks, Autoimmune diseases, Carotid artery stenosis, Chondrocalcinosis, Common carotid artery stenosis, Congenital pectus carinatum, Dwarfism, External carotid artery stenosis, Hearing loss, Hypercalcemia, Hyperphosphatasemia with bone disease, Hyperphosphatemia, Hypertension, Hyperuricemia, Hypothyroidism, Internal carotid artery stenosis, Macrocephaly, Melanocytic nevus, Milk-alkali syndrome, Optic atrophy, Osteoporosis, Osteosclerosis, Paget disease, Rheumatoid arthritis, UremiaView all (10 more) |
|
340
|
|
|
Taste 2 receptor member 13 |
T2R13, TRB3 |
|
