|
351
|
|
|
Histidine rich carboxyl terminus 1 |
LGLL338, PRO537, UNQ338 |
|
|
352
|
|
|
Helicase like transcription factor |
HIP116, HIP116A, HLTF1, RNF80, SMARCA3, SNF2L3, ZBU1 |
|
|
353
|
|
|
HNF1 homeobox A |
HNF-1-alpha, HNF-1A, HNF1, HNF1alpha, HNF4A, IDDM20, LFB1, MODY3, TCF-1, TCF1 |
Autoimmune diabetes, Chromophobe carcinoma, Hyperinsulinemic hypoglycemia, Pancreatic hypoplasia, Coronary artery disease, Coronary heart disease, Diabetes mellitus, Brittle diabetes mellitus, Diabetic nephropathy, Exocrine pancreatic insufficiency, Gout, Gouty arthritis, Hepatic adenomas, Hepatocellular adenoma, Hyperglycemia, Hyperinsulinism, Hypoglycemia, Hypoinsulinemia, Ketosis, Kidney disease, Liver carcinoma, Mason type diabetes, Mental retardation, Monogenic diabetes, Hypotonia, Obesity, Pancreatic carcinoma, Papillary renal carcinoma, Polycystic ovary syndrome, Reactive hypoglycemia, Renal carcinoma, Renal cyst, Retinal diseasesView all (18 more) |
|
354
|
|
|
HNF1 homeobox B |
ADTKD3, FJHN, HNF-1-beta, HNF-1B, HNF1beta, HNF2, HPC11, LF-B3, LFB3, MODY5, RCAD, T2D, TCF-2, TCF2, VHNF1 |
17q12 deletion syndrome, Arthritis, Asthenozoospermia, Autism, Benign prostatic hyperplasia, Bilateral multicystic dysplastic kidney, Breast carcinoma, Cerebral atrophy, Cerebral cortical atrophy, Cholestasis, Chromophobe carcinoma, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Absent vas deferens, Congenital atresia of vas deferens, Pancreatic hypoplasia, Cryptorchidism, Developmental delay, Diabetes mellitus, Dwarfism, Endometrial neoplasms, Endometrial carcinoma, Exocrine pancreatic insufficiency, Fanconi syndrome, Fatty liver, Gout, Horseshoe kidney, Hyperuricemia, Hyperuricemic nephropathy, Hypomagnesemia, Hypospadias, Hypothyroidism, Kidney disease, Language disorders, Lung carcinoma, Lung adenocarcinoma, Malocclusion, Mason type diabetes, Mental retardation, Monogenic diabetes, Multicystic renal dysplasia, Nasopharyngeal carcinoma, Nephrolithiasis, Ovarian cancer, Ovarian neoplasm, Ovarian serous adenocarcinoma, Ovarian adenocarcinoma, Ovarian endometrioid carcinoma, Pancreatic carcinoma, Papillary cystadenoma of the epididymis, Papillary renal carcinoma, Hypomagnesemia with hypocalciuria, Prostatic neoplasms, Prostate cancer, Renal agenesis, Renal carcinoma, Renal cyst, Renal cysts and diabetes syndrome, Renal dysplasia, Renal glomerular disease, Renal insufficiency, Spermatocele, Subcortical cerebral atrophy, Testicular germ cell tumor, Tubulointerstitial kidney disease, Unilateral multicystic dysplastic kidney, UreteroceleView all (53 more) |
|
355
|
|
|
Heat shock protein 90 beta family member 1 |
ECGP, GP96, GRP94, HEL-S-125m, HEL35, TRA1 |
|
|
356
|
|
|
Hepatocellular carcinoma up-regulated long non-coding RNA |
HCCAT1, LINC00078, NCRNA00078 |
|
|
357
|
|
|
Histone cell cycle regulator |
DGCR1, TUP1, TUPLE1 |
22q11 deletion syndrome, 22q11 partial monosomy syndrome, 22q11.2 deletion syndrome, Acne, Acrocephaly, Anxiety disorder, Arachnodactyly, Arrhinencephaly, Arthritis, Asthma, Asymmetric crying face association, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bowel incontinence, Cataract, Choanal atresia, Cholelithiasis, Chronic obstructive pulmonary disease, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of thymus, Congenital malrotation of intestine, Conotruncal anomaly face syndrome, Corneal neovascularization, Cryptorchidism, Developmental delay, Digeorge syndrome, Dwarfism, Dysphasia, Gastroesophageal reflux disease, Glaucoma, Hearing loss, Hirschsprung disease, Hydrocephalus, Hyperthyroidism, Hypoparathyroidism, Hypospadias, Hypothyroidism, Immunologic deficiency syndromes, Impaired cognition, Imperforate anus, Laryngomalacia, Major affective disorder, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Multiple renal cysts, Myelomeningocele, Obesity, Optic atrophy, Otitis media, Patent ductus arteriosus, Persistent truncus arteriosus, Platybasia, Polycystic kidney disease, Polydactyly of toes, Posterior embryotoxon, Ptosis, Renal hypoplasia, Schizophrenia, Scoliosis, Seborrheic dermatitis, Shprintzen syndrome, Specific learning disorder, Strabismus, Tetralogy of fallot, Tricuspid atresia, Uterine anomalies, Ventricular septal defect, Vesicoureteral reflux, Vulval varicesView all (62 more) |
|
358
|
|
|
Heat shock protein 90 alpha family class A member 5, pseudogene |
HSP90Ae |
|
|
359
|
|
|
Hydroxysteroid 17-beta dehydrogenase 8 |
D6S2245E, FABG, FABGL, H2-KE6, HKE6, KE6, RING2, SDR30C1, dJ1033B10.9 |
|
|
360
|
|
|
High mobility group nucleosome binding domain 5 |
NBP-45, NSBP1 |
|
