|
551
|
|
|
RNA polymerase II subunit J |
POLR2J1, RPB11, RPB11A, RPB11m, hRPB14 |
|
|
552
|
|
|
Proopiomelanocortin |
ACTH, CLIP, LPH, MSH, NPP, OBAIRH, POC |
Acanthosis nigricans, Adrenal cortex diseases, Adrenocorticotropic hormone deficiency, Amnesia, Athetoid cerebral palsy, Autism, Behavior disorders, Bipolar disorder, Bright disease, Cardiomyopathy, Catalepsy, Cerebral palsy, Cerebral palsy, diplegic, Cholestasis, Chondrocalcinosis, Chromophobe carcinoma, Clonic seizures, Congenital cerebral palsy, Congestive heart failure, Cryptogenic tonic-clonic epilepsy, Cryptogenic west syndrome, Cushing`s syndrome, Cystitis, Diabetes insipidus, Diabetes mellitus, Disorder of eye, Ectopic acth secretion syndrome, Epilepsy, Facial paralysis, Fatty liver, Femur head necrosis, Functional gastrointestinal disorders, Gastrointestinal diseases, Glomerulonephritis, Gonadotropin deficiency, Gouty arthritis, Heart failure, Hyperbilirubinemia, Hyperinsulinism, Hypertension, Hypertrophic cardiomyopathy, Hypoglycemic seizures, Hypogonadism, Hypopigmentation disorder, Hypotonic seizures, Immune system diseases, Inappropriate acth secretion syndrome, Isolated somatotropin deficiency, Jackknife seizures, Jacksonian seizure, Kidney disease, Kidney failure, Kidney stone, Spastic diplegia, Liver failure, Long qt syndrome, Manic disorder, Melancholia, Melanoma, Mental disorders, Mental depression, Monoplegic cerebral palsy, Multiple sclerosis, Myasthenia gravis, Myocardial diseases, Myocardial infarction, Myocardial ischemia, Myoclonic astatic epilepsy, Myoclonic encephalopathy, Myoclonic epilepsy, Myotonia levior, Nephrocalcinosis, Obesity, Opsoclonus-myoclonus syndrome, Osteoporosis, Pancreatic diseases, Papillary renal carcinoma, Penile diseases, Pituitary dependent hypercortisolism, Proopiomelanocortin deficiency, Pyogenic sacroiliitis, Renal carcinoma, Acute kidney insufficiency, Renal tubular necrosis, Restless legs syndrome, Rhabdomyoma, Sacroiliitis, Salaam seizures, Adrenal insufficiency, Hypothyroidism, Seizure, Septic sacroiliitis, Short sleeper syndromes, Sick sinus syndrome, Sinus node dysfunction, Sleep disorders, Sleep wake disorders, Somatotropin deficiency, Spasmus nutans, Spastic cerebral palsy, Subaortic stenosis, Symptomatic west syndrome, Synovial hypertrophy, Synovitis, Tonic-clonic epilepsy, Tumoral calcinosis, West syndromeView all (92 more) |
|
553
|
|
|
Paraoxonase 1 |
ESA, MVCD5, PON |
Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Anxiety disorder, Atherosclerosis, Atherosclerotic parkinsonism, Autism, Bipolar disorder, Brain neoplasms, Intracranial neoplasm, Cardiovascular diseases, Cerebral primitive neuroectodermal tumor, Cholestasis, Congestive heart failure, Coronary arteriosclerosis, Coronary artery disease, Coronary artery vasospasm, Coronary heart disease, Coronary syndrome, Diabetes mellitus, Diabetic nephropathy, Diabetic retinopathy, Ependymoblastoma, Fatty liver, Glomerulonephritis, Glomerulosclerosis, Heart diseases, Heart failure, Hematologic neoplasms, Hematopoietic neoplasms, Hemorrhoids, Hypercholesterolemia, Hyperhomocysteinemia, Hyperlipoproteinemia, Hyperthyroidism, Laryngospasm, Lateral sclerosis, Lung neoplasms, Lung cancer, Lymphoma, Marginal periodontitis, Medulloepithelioma, Melancholia, Mental depression, Metabolic diseases, Metabolic syndrome, Mood swings, Myocardial infarction, Nephrotic syndrome, Neuroectodermal tumors, Parkinson disease, Periodontal diseases, Persian gulf syndrome, Prostatic neoplasms, Prostate cancer, Rachischisis, Respiratory failure, Rheumatoid arthritis, Schizophrenia, Spina bifida, Spongioblastoma, Status dysraphicusView all (46 more) |
|
554
|
|
|
Paraoxonase 2 |
- |
|
|
555
|
|
|
Proline rich 13 |
TXR1 |
|
|
556
|
|
|
Paraoxonase 3 |
- |
|
|
557
|
|
|
Cytochrome p450 oxidoreductase |
CPR, CYPOR, P450R |
Acne, Adrenogenital syndrome, Ambiguous genitalia, Antley-bixler syndrome, Antley-bixler syndrome with genital anomalies and disordered steroidogenesis, Arachnodactyly, Arnold-chiari malformation, Atresia of vagina, Atrial septal defect, Urinary bladder cancer, Bladder neoplasm, Brachycephaly, Bronchomalacia, Carpal synostosis, Choanal atresia, Clinodactyly, Congenital adrenal hyperplasia, Congenital camptodactyly, Coronal craniosynostosis, Craniosynostosis, Cryptorchidism, Deficiency of testosterone biosynthesis, Dwarfism, Ectopic adrenal gland, Enlarged polycystic ovaries, Female sexual dysfunction, Frontal bossing, Gliosarcoma, Hearing loss, Horseshoe kidney, Hydrocephalus, Hypertension, Hypertrophy of clitoris, Hypoplasia of vagina, Hypospadias, Laryngomalacia, Learning disorders, Male pseudohermaphroditism, Mental retardation, Microcephaly, Osteoporosis, Penis agenesis, Polycystic ovary syndrome, Premature adrenarche, Proptosis, Radioulnar synostosis, Ramer ladda syndrome, Scoliosis, Stenosis of external auditory canal, Synostotic posterior plagiocephaly, Tarsal coalition, Vertical talus, Vesicovaginal fistulaView all (38 more) |
|
558
|
|
|
POU class 1 homeobox 1 |
CPHD1, GHF-1, PIT1, POU1F1a, Pit-1 |
Agenesis of corpus callosum, Central hypothyroidism, Congenital exomphalos, Congenital hypothyroidism, Developmental delay, Dwarfism, Dyssomnia, Ectopic anterior pituitary gland, Frontal bossing, Holoprosencephaly, Hypoglycemia, Hypogonadotropic hypogonadism, Hypothyroidism, Isolated growth hormone deficiency, Macroglossia, Mental retardation, Obsessive-compulsive disorder, Oral cleft, Osteopenia, Osteoporosis of vertebrae, Panhypopituitarism, Pituitary dwarfism, Pituitary hormone deficiency, Polydactyly, Septo-optic dysplasia, Sleep disorders, Tourette syndromeView all (12 more) |
|
559
|
|
|
Protein arginine methyltransferase 7 |
SBIDDS |
Acanthosis nigricans, Astigmatism, Brachydactyly, Congenital epicanthus, Developmental delay, Dwarfism, Fatty liver, Frontal bossing, High palate, Mental retardation, Microcephaly, Obesity, Pseudohypoparathyroidism, Renal hypoplasia, Short stature, brachydactyly, intellectual developmental disability, and seizures, Skeletal dysplasia, StrabismusView all (2 more) |
|
560
|
|
|
POU class 2 homeobox associating factor 1 |
BOB1, OBF-1, OBF1, OCAB |
Biliary cholangitis, Biliary cirrhosis, Celiac disease, Cirrhosis, Conjugated hyperbilirubinemia, Dermatographic urticaria, Gastrointestinal inflammation, Hodgkin disease, Hypoalbuminemia, Liver carcinoma, Liver failure, Liver fibrosis, Osteoporosis, Portal hypertension |
