Related by context. All words. (Click for frequent words.) 69 ADPKD 67 myeloproliferative neoplasms 66 NAFLD 65 basal cell nevus syndrome 65 Hashimoto thyroiditis 65 nonalcoholic steatohepatitis NASH 65 AAT deficiency 64 liver scarring 64 Hurler syndrome 64 SSc 64 hepatic cirrhosis 64 myopathies 64 Sjögren syndrome 63 rheumatic disease 63 sporadic ALS 63 MGUS 63 pulmonary hypertension PH 63 lichen planus 63 systemic lupus erythematosus SLE 63 familial adenomatous polyposis 63 gastric carcinoma 63 cirrhotic 63 underlying pathophysiology 63 ABCB1 63 torsade de pointes 62 disease NAFLD 62 myelodysplasia 62 T1DM 62 chronic granulomatous disease 62 basal cell carcinoma BCC 62 familial ALS 62 diabetic nephropathy 62 hereditary predisposition 62 monogenic 62 TTR amyloidosis 62 familial pancreatic cancer 62 hyperinsulinemia 62 FSGS 62 APOL1 62 untreated celiac disease 62 G6PD deficiency 62 proliferative diabetic retinopathy 62 thyroid dysfunction 62 atherothrombosis 62 hyperammonemia 62 alcoholic hepatitis 62 Cryptococcus neoformans 62 nonalcoholic steatohepatitis 62 antiphospholipid syndrome 62 lysosomal storage diseases 62 PsA 62 polycystic ovary syndrome 62 nonhereditary 61 NAGS deficiency 61 lipid abnormalities 61 dyskeratosis congenita 61 prostate cancer CaP 61 ORMDL3 61 colorectal carcinoma 61 chronic pancreatitis 61 TMEM#B 61 thyrotoxicosis 61 neurological manifestations 61 JMML 61 fructose intolerance 61 IL#R 61 recurrent miscarriage 61 genetic syndromes 61 juvenile idiopathic arthritis 61 EoE 61 systemic scleroderma 61 gene polymorphisms 61 cardiac hypertrophy 61 diabetic kidney 61 atopic eczema 61 thrombophilia 61 airway hyperresponsiveness 61 liver fibrosis 61 gallstone disease 61 diabetes mellitus DM 61 cirrhosis liver failure 61 Alport syndrome 61 hepatic steatosis 61 inherited mutations 61 narcolepsy cataplexy 61 MELAS 61 hamartomas 61 C. trachomatis 61 CHD7 61 Clusterin 61 biochemical abnormalities 61 genetic polymorphisms 61 transfusion syndrome 61 pyelonephritis 61 adenocarcinomas 61 Coeliac disease 60 TCF#L# gene 60 metabolic abnormalities 60 leiomyomas 60 haematologic 60 ANCA associated 60 neuropathologic 60 MYH9 gene 60 Pulmonary hypertension 60 underlying vasculopathy 60 autosomal dominant disorder 60 hepatorenal syndrome 60 cystic fibrosis chronic pancreatitis 60 nephritis 60 atrophic gastritis 60 renal cell carcinomas 60 metabolic disturbances 60 LRP5 60 Fanconi syndrome 60 secondary hyperparathyroidism 60 T2DM 60 glomerulonephritis 60 FTLD 60 NF1 60 neuropsychiatric disorder 60 neoplasias 60 endometrial hyperplasia 60 paraganglioma 60 Nonalcoholic fatty liver 60 anemias 60 pancreatic adenocarcinoma 60 familial hypercholesterolemia 60 lung fibrosis 60 bladder cancers 60 liver histology 60 GPC5 60 atypical hemolytic uremic syndrome 60 PCOD 60 polycystic ovary syndrome PCOS 60 Cowden syndrome 60 HNPCC 60 PAOD 60 osteosarcomas 60 hypercalciuria 60 malignant lymphoma 60 paraneoplastic 60 Leukemias 60 UGT#A# * 60 carcinoid 60 GISTs 60 testicular germ cell 60 Vitamin B# deficiency 60 hepatic fibrosis 60 hyperphenylalaninemia HPA due 60 bulimia nervosa 60 intestinal polyps 60 WNK1 60 Carcinoid tumors 60 neuritic 60 HLA DRB1 60 Systemic lupus erythematosus SLE 60 alanine aminotransferase ALT 60 parkinsonism 60 systemic lupus erythematosus 60 mitochondrial dysfunction 60 leukemias lymphomas 60 Sezary syndrome 60 Prostatitis 60 polycystic kidneys 60 clinicopathological 60 iron overload 60 autoimmune thyroiditis 60 ectodermal dysplasia 60 kidney urologic 60 systemic autoimmune 59 lactase deficiency 59 atopic 59 alpha1 antitrypsin deficiency 59 Bronchiectasis 59 Von Willebrand disease 59 Candidiasis 59 Chronic lymphocytic leukemia 59 sortilin 59 Gorlin syndrome 59 phenylketonuria 59 euthymic patients 59 Helicobacter pylori infection 59 Lafora disease 59 recurrent miscarriages 59 erythropoietic 59 calcium oxalate stones 59 primary hyperparathyroidism 59 SGPT 59 essential thrombocythemia 59 Primary biliary cirrhosis 59 neurodegenerative disorder 59 neurofibromas 59 spinocerebellar ataxia 59 reflux disease 59 imatinib resistance 59 germline mutations 59 serum phosphate 59 Genetic predisposition 59 aneuploidies 59 vascular dysfunction 59 lymphocytic 59 cause cardiac channelopathies 59 hematopoietic cancers 59 neuro degenerative disease 59 myelofibrosis polycythemia vera 59 HBeAg negative 59 elevated ALT 59 myeloproliferative diseases 59 bacterial prostatitis 59 Atopic dermatitis 59 cholestasis 59 atypical hyperplasia 59 KRAS oncogene 59 pernicious anemia 59 IPAH 59 lobular carcinoma 59 breast endometrial 59 allograft rejection 59 AAT Deficiency 59 bronchopulmonary dysplasia BPD 59 dominantly inherited 59 hepatocellular carcinomas 59 hypothalamic pituitary adrenal axis 59 myeloproliferative disorders 59 inflammatory bowel syndrome 59 familial clustering 59 GSTT1 59 carcinoid tumor 59 abnormal uterine bleeding 59 dysglycemia 59 Waldenstrom macroglobulinemia 59 allogeneic HSCT 59 malignant lymphomas 59 IGFBP2 59 cardiovascular calcification 59 lymphoproliferative disorders 59 pheochromocytoma 59 carcinoid tumors 59 hypermethylation 59 Bardet Biedl syndrome 59 thyroid deficiency 59 gene MECP2 59 dysregulated 59 Inflammatory bowel diseases 59 progressive neurodegenerative disorder 59 lysosomal storage disease 59 HER2 overexpression 59 inflammatory bowel diseases 59 systemic amyloidosis 59 Non Alcoholic Steatohepatitis 59 urethritis 59 paragangliomas 59 papillary renal cell carcinoma 59 Wernicke Korsakoff syndrome 59 nephrogenic fibrosing dermopathy 59 cryptogenic 59 anti fibrotic 59 autonomic dysfunction 59 cardiac fibrosis 59 hypereosinophilic syndrome 59 oesophageal adenocarcinoma 59 neurogenic 59 intracranial hemorrhage ICH 59 T2D 59 ataxias 59 Pulmonary arterial hypertension 59 Elevated serum 59 neuropathological 59 discoid lupus 59 gluten sensitive enteropathy 59 Chronic Prostatitis 59 Myasthenia gravis 59 lymphangioleiomyomatosis LAM 58 MALT lymphoma 58 lung adenocarcinoma 58 bacteraemia 58 clefting 58 GIST tumors 58 celiac sprue 58 subependymal giant cell 58 etiologic factors 58 Cholangiocarcinoma 58 Beta thalassemia 58 Iron deficiency anemia 58 Wilms tumors 58 idiopathic PAH 58 chlamydial infection 58 deletion 5q 58 PTEN mutations 58 hereditary deafness 58 rheumatic disorders 58 SNCA 58 mesotheliomas 58 Severe Primary IGFD 58 chromosomal rearrangement 58 pancreatic neuroendocrine tumors 58 node metastases 58 chronic hepatitis 58 p# activation 58 hematological diseases 58 Neurofibromatosis type 58 PTPN# 58 Celiac sprue 58 genetic determinants 58 p# mutations 58 mycosis fungoides 58 LRRK2 gene 58 MPS VI 58 genetic polymorphism 58 Parkinson Disease PD 58 urothelial cancer 58 eosinophilic 58 spontaneous remission 58 5q deletion 58 non alcoholic steatohepatitis 58 post transplant lymphoproliferative 58 histological subtype 58 motor neuron degeneration 58 Sjogren Syndrome 58 Dysregulation 58 Aortic stenosis 58 EBV infection 58 colorectal cancer CRC 58 androgenic alopecia 58 filaggrin 58 Six3 58 lupus erythematosus 58 metastatic malignant 58 androgen excess 58 IgA deficiency 58 adrenocortical cancer 58 renal fibrosis 58 autoinflammatory diseases 58 tumoral 58 astrocytomas 58 K ras mutations 58 polyomavirus nephropathy 58 subclinical hypothyroidism 58 autosomal dominant polycystic kidney 58 mucinous 58 spontaneous bacterial peritonitis 58 CP CPPS 58 hyperinsulinism 58 autosomal recessive genetic 58 CYP#D# 58 ductal breast cancer 58 orchitis 58 1 diabetes T1D 58 CC genotype 58 Lupus nephritis 58 Irritable bowel syndrome IBS 58 metaplasia 58 haematopoietic 58 chronic eosinophilic leukemia 58 Langerhans cell histiocytosis 58 leukemia ALL 58 cutaneous melanoma 58 myeloperoxidase 58 NF2 58 behavioral disinhibition 58 unresectable tumors 58 atherosclerotic lesions 58 susceptibility gene 58 arrhythmogenic right 58 cerebrospinal fluid CSF 58 hyperprolactinemia 58 JAK2 enzyme 58 Joubert syndrome 58 exocrine 58 PDGFR 58 pathophysiologic 58 pituitary adenoma 58 amyloid deposition 58 steatosis 58 Kufs disease 58 Epstein Barr virus EBV 58 kidney insufficiency 58 hydrops 58 HeFH 58 FGFs 58 CYP#C# [002] 58 Peutz Jeghers syndrome 58 epithelial tumors 58 inflammatory bowel disease 58 functional polymorphism 58 generalized epilepsy 58 susceptibility loci 58 hereditary hemochromatosis 58 neuropsychiatric disorders 58 membranous nephropathy 58 chorioamnionitis 58 vWD 58 endothelial dysfunction 58 SIADH 58 leukaemias 58 hepatocellular carcinoma 58 posttransplant 58 hyperplastic 58 anterior uveitis 58 nonmelanoma skin cancers 58 colorectal carcinogenesis 58 bullous 58 HIV HCV coinfected 58 penetrance 58 thyroiditis 58 Vitamin D insufficiency 58 LQTS 58 lactose malabsorption 58 cystatin C 58 keloid scars 58 overt nephropathy 58 GNAQ 58 premalignant lesions 58 benign breast 58 chronic periodontitis 58 motor neuron diseases 58 Nonalcoholic Fatty Liver Disease 58 neuroendocrine cancers 58 dysmotility 58 ductal adenocarcinoma 58 COL#A# 58 GBA mutations 58 Papillary 58 granulomatous 58 primary ciliary dyskinesia 58 macroalbuminuria 58 carbohydrate metabolism 58 myeloid leukemia 58 microalbuminuria 58 leukemia AML 58 MPGN 58 inducible nitric oxide synthase 58 prostate adenocarcinoma 58 microdeletion 58 IDH1 mutation 58 WDR# 58 Chronic fatigue 58 mitochondrial disorders 58 immunosuppressive therapies 58 decompensated liver disease 58 elevated triglyceride levels 58 allogeneic hematopoietic stem cell 58 colorectal adenocarcinoma 58 de ath 58 carotid stenosis 58 CYP#B# 58 nonalcoholic fatty liver 58 CYT# potent vascular disrupting 58 Sclerosing 58 myositis 58 myelodysplastic syndrome MDS 58 eosinophilic esophagitis 58 type 1diabetes 57 lupus scleroderma 57 elevated uric acid 57 MPS IVA 57 erythematosus 57 LHON 57 leiomyoma 57 stress cardiomyopathy 57 monoclonal gammopathy 57 myotonic dystrophy 57 PCNSL 57 Raf MEK ERK 57 idiopathic myelofibrosis 57 bronchopulmonary dysplasia 57 allogeneic transplants 57 hypothalamic amenorrhea 57 PTHrP 57 MSH2 57 elevated LDL cholesterol 57 BRAF V#E 57 smoldering myeloma 57 HNSCC 57 incidentalomas 57 purpura 57 chronic GVHD 57 chromosomal abnormalities 57 cytomegalovirus infection 57 thyrotropin 57 enterocolitis 57 MTHFR 57 TEAEs 57 demyelinating 57 adrenal function 57 Myelodysplastic Syndrome MDS 57 hypovitaminosis D 57 chronic autoimmune disorder 57 SIBO 57 bronchogenic carcinoma 57 Idiopathic 57 AA Amyloidosis 57 Fibrosis 57 adenomatous polyps 57 acute myelogenous leukemia AML 57 chronic idiopathic 57 hematopoietic cell 57 Leber Hereditary Optic Neuropathy 57 cranial irradiation 57 idiopathic thrombocytopenic purpura ITP 57 proto oncogene 57 hyperkalemia 57 gastrointestinal stromal tumor 57 Heavy menstrual bleeding 57 Cushing syndrome 57 nephrogenic 57 activin 57 myeloproliferative 57 Myelodysplastic Syndrome 57 infarcts 57 Epstein Barr Virus EBV 57 airway remodeling 57 mosaicism 57 UVB induced 57 Acute Myeloid Leukaemia 57 geographic atrophy 57 muscular dystrophy cystic fibrosis 57 molar pregnancy 57 metastatic neuroendocrine tumors 57 Hurthle cell 57 epididymitis 57 testicular tumors 57 bacterial vaginosis BV 57 S. maltophilia 57 Pseudomonas aeruginosa infections 57 somatic mutation 57 ursodeoxycholic acid 57 Endothelial dysfunction 57 bridging fibrosis 57 chronic HBV infection 57 neoplastic 57 Crohn disease CD 57 hyperparathyroidism 57 Adenomas 57 mastocytosis 57 fibrotic disease 57 androgenetic alopecia 57 CDH1 57 testicular cancers 57 neuropsychiatric diseases 57 sarcomatoid 57 Hyperthyroidism 57 hirsutism 57 B7 H3 57 nephrolithiasis 57 #q# [001] 57 myocardial fibrosis 57 SHPT 57 HER2 expression 57 breast cancer metastasis 57 mtDNA mutations 57 heterotaxy 57 amyloid deposits 57 Thrombocytopenia 57 coronary artery atherosclerosis 57 gastric adenocarcinoma 57 CYP# [002] 57 Genetic variants 57 Chiari malformation 57 primary aldosteronism 57 proliferative retinopathy 57 PARP inhibition 57 multisystem disease 57 decompensated cirrhosis 57 nonischemic 57 glutamic acid decarboxylase 57 metabolic acidosis 57 Magnesium deficiency 57 methylation patterns 57 Wilms tumor 57 ZNF# 57 giant cell arteritis 57 esophagogastric 57 extramedullary 57 chronic myeloid 57 uveal melanoma 57 tuberous sclerosis complex 57 Candida infection 57 etiologic 57 pre eclampsia 57 pancreatic endocrine 57 hypoperfusion 57 POAG 57 STAT4 57 renal allograft 57 pleural mesothelioma 57 Chronic Fatigue Syndrome CFS 57 dystrophies 57 de novo mutations 57 PTEN gene 57 diagnostic biomarker 57 IKZF1 57 rs# [002] 57 serous ovarian cancer 57 premature ovarian 57 alanine aminotransferase 57 stone formers 57 adenoma 57 optica 57 Congenital Muscular Dystrophy 57 histone deacetylases 57 1 Antitrypsin Deficiency 57 malignant pleural mesothelioma 57 hepatocellular carcinoma HCC 57 psoriatic arthritis PsA 57 vulvodynia 57 epigenetic changes 57 microvascular disease 57 Atypical Hemolytic Uremic Syndrome 57 autoimmune disease 57 eccrine 57 neurocognitive impairment 57 fibrogenesis 57 neuronal dysfunction 57 myeloid 57 somatization disorder 57 EXJADE 57 alcoholic fatty liver 57 epigenetic alterations 57 interstitial nephritis 57 choriocarcinoma 57 oncogenesis 57 autoimmune thyroid 57 cholangiocarcinoma 57 Chronic pancreatitis 57 sCJD 57 muscular dystrophies 57 thalassemia sickle cell 57 G6PD 57 Pancreatic 57 NOMID 57 cell adhesion molecule 57 demyelination 57 excess uric acid 57 precancerous condition 57 esophageal squamous cell carcinoma 57 pentoxifylline 57 Relapsing remitting MS 57 idiopathic pulmonary arterial hypertension 57 von Hippel Lindau 57 FASPS 57 colorectal adenoma 57 nutlin 3a 57 Squamous 57 liver metastasis 57 breast cancer subtypes 57 familial adenomatous polyposis FAP 57 aetiology 57 vasculitis 57 abdominal adiposity 57 monozygotic twin 57 H pylori 57 hereditary spastic paraplegia 57 polymorphic ventricular tachycardia 57 genetic loci 57 OSAHS 57 Henoch purpura 57 #q#.# deletion syndrome 57 CTAP# Capsules 57 diabetic gastroparesis 57 Angiotensin II 57 papillary carcinoma 57 pathophysiological mechanisms 57 pathogenic mechanisms 57 aneurysmal subarachnoid hemorrhage 57 histologic subtype 57 metastatic gastric 57 fatal neurodegenerative disorder 57 hyperoxaluria 57 ciliopathies 57 preserved ejection fraction 57 anaplastic lymphoma kinase 57 Atopic eczema 57 proliferative disorders 57 intestinal inflammation 57 Glucocorticoids 57 antibody mediated 57 CYP#D# gene 57 GH deficiency 57 PCa 57 Polycystic Ovary Syndrome 57 serum selenium 57 Autoimmune disorders 57 neuroblastomas 56 EGFR mutations 56 urothelial 56 Zinc deficiency 56 chromosomal anomalies 56 gastro oesophageal reflux 56 Hereditary angioedema 56 vaginitis 56 prolonged QT interval 56 protein misfolding diseases 56 mesangial 56 synovial fibroblasts 56 pyloric stenosis 56 Venous thromboembolism 56 Mitochondrial dysfunction 56 Friedreich ataxia 56 breast carcinomas 56 severe congenital neutropenia 56 smoldering multiple myeloma 56 folate metabolism 56 Cytogenetic 56 Leber congenital amaurosis LCA 56 PGDH 56 chronicity 56 1 proteinase inhibitor 56 colonic mucosa 56 Ribavirin causes 56 unknown etiology 56 aldehyde dehydrogenase 56 gouty arthritis 56 overactive bladder symptoms 56 Systemic lupus erythematosus 56 beta thalassemia 56 #q# deletion 56 autosomal dominant 56 idiopathic pulmonary 56 thyroid abnormalities 56 circulating endothelial cells 56 gastro esophageal reflux 56 Ovarian cysts 56 enzyme deficiency 56 bowel cancers 56 interleukins 56 Epstein Barr Virus 56 fibrosis 56 chronic prostatitis 56 acromegaly 56 dermatologic reactions 56 bronchiectasis 56 Leydig cell 56 gastroesophageal reflux GERD 56 HbF 56 herpesviruses 56 Hypotension 56 seminomas 56 congenital deficiency 56 microangiopathy 56 #q#.# [001] 56 optic neuropathy 56 hemolytic anemia 56 juvenile idiopathic arthritis JIA 56 MC1R 56 CMV infection 56 intravenous bisphosphonates 56 chronic rhinosinusitis 56 sFlt 1 56 gastric cancers 56 atherosclerotic disease 56 chromosomal instability 56 hyperglycaemia 56 Upregulation 56 persistent pulmonary hypertension 56 anovulation 56 NPHP 56 Cockayne syndrome 56 Acne Rosacea 56 alpha synuclein protein 56 medulloblastomas 56 trans retinoic acid 56 VIPR2 56 CYP #A# 56 STK# gene 56 left ventricular diastolic 56 Irritable bowel syndrome 56 folate deficiency 56 pretransplant 56 excitotoxicity 56 demyelinating disease 56 hepatic liver 56 relapsed leukemia 56 circadian genes 56 polymyalgia rheumatica 56 Male pattern baldness 56 spastic diplegia 56 atypical Hemolytic Uremic Syndrome 56 lymphomas leukemias 56 cell carcinomas 56 myelodysplastic myeloproliferative diseases 56 renal scarring 56 renovascular hypertension 56 immunocompetent 56 neurotrophic 56 frontotemporal dementia 56 valvular heart disease 56 Crohn disease 56 hypocalcaemia 56 autosomal dominant inheritance 56 diabetic microvascular complications 56 thrombocytopenic 56 papillary thyroid carcinoma 56 ovarian pancreatic 56 lung metastasis 56 Pemphigus 56 benign proliferative breast 56 malignant pleural effusion 56 medium chain acyl 56 sulfasalazine 56 DNA methylation patterns 56 Fas ligand 56 microvascular dysfunction 56 liver cirrhosis 56 clinicopathologic 56 neovascularization 56 carcinoid syndrome 56 atherosclerotic cardiovascular disease 56 neurocognitive deficits 56 homozygous familial hypercholesterolemia 56 hypothalamic pituitary 56 Morquio 56 ependymomas 56 malabsorption 56 Fanconi Anemia 56 chromosome abnormality 56 Basal Cell 56 CYP#A# gene 56 arthropathy 56 mitogen activated protein kinase 56 proctitis 56 allogeneic bone marrow 56 IgA nephropathy 56 graft occlusion 56 CEACAM1 56 CCR5 delta# 56 urethral stricture 56 Li Fraumeni syndrome 56 vascular abnormalities 56 serum lipid levels 56 Becker muscular dystrophy 56 biologic pathways 56 glucose homeostasis 56 causative genes 56 liver disease 56 dopamine receptor gene 56 amnestic MCI 56 mTOR mammalian target 56 dermopathy 56 metabolic abnormality 56 VCFS 56 polycystic ovarian syndrome PCOS 56 grade cervical intraepithelial 56 clinico pathological 56 Pre eclampsia 56 hypercoagulable 56 squamous cell lung cancer 56 systolic hypertension 56 chronic gastritis 56 hepatocellular 56 Genetic variations 56 vascular endothelial 56 NKX2 56 cortical dysplasia 56 ankylosing spondylitis AS 56 ovarian carcinoma 56 subclinical hyperthyroidism 56 calcium oxalate 56 malignant transformation 56 lupus nephritis 56 APOE ε4 56 osteopontin 56 neuroendocrine 56 Treg cell 56 rheumatoid 56 prognostic markers 56 clinically heterogeneous 56 premalignant 56 BCL#A 56 multiorgan 56 fibromyalgia syndrome 56 situ LCIS 56 sporadic Creutzfeldt Jakob 56 relapsed MM 56 colorectal adenomas 56 variceal bleeding 56 primary immunodeficiency PI 56 seminoma 56 invasive carcinoma 56 pilocytic astrocytomas 56 Non Alcoholic Fatty 56 Wegener granulomatosis 56 VKORC1 56 thromboembolic disease 56 autoantibodies 56 graft dysfunction 56 renal disease 56 gene polymorphism 56 Sjogren syndrome 56 ADAM# 56 hyperalgesia 56 SLC#A# [002] 56 autoimmune 56 lymphocyte activation 56 breast carcinoma 56 fatal neurodegenerative 56 γ secretase 56 autosomal recessive disorder 56 T#I [002] 56 recurrent acute pancreatitis 56 nerve degeneration 56 postoperative atrial fibrillation 56 SCD1 56 hormone aldosterone 56 developmental abnormalities 56 Hutchinson Gilford progeria 56 neuroblastoma tumor 56 Keratitis 56 neurofibroma 56 achalasia 56 BRCA1 BRCA2 56 adrenal cortex 56 pemphigus 56 coagulation abnormalities 56 causal variants 56 apoE4 56 leukemia CLL 56 apoptotic pathway 56 Brugada syndrome 56 histologies 56 cardiac insufficiency 56 carbohydrate intolerance 56 potentially modifiable 56 fluoroquinolone resistance 56 lymphomas 56 amenorrhoea 56 nonsense mutations 56 Bacterial vaginosis 56 Prehypertension 56 Polycystic ovary syndrome PCOS 56 Retinitis pigmentosa 56 Hurler Syndrome 56 interstitial fibrosis 56 epithelioid 56 endocrine tumors 56 tumor histology 56 vasculopathy 56 elevated CRP 56 nasopharyngeal carcinoma 56 basal cell carcinomas 56 undiagnosed celiac disease 56 pathogenetic 56 renal tumors 56 Hirschsprung disease 56 NAT2 56 Wiskott Aldrich syndrome 56 Inflammatory bowel disease 56 acute myeloid 56 Galectin 3 56 impaired glucose metabolism 56 epilepsies 56 cerebral vasospasm 56 bladder carcinoma 56 hematological parameters 56 molecular abnormalities 56 obesity insulin resistance 56 cholelithiasis 56 esophagitis 56 hypermethylated 56 Leber hereditary optic neuropathy 56 seropositive patients 56 Nephrotic Syndrome 56 impair fertility 56 asthma rhinitis 56 cardiomyopathies 56 normal karyotype 56 ERK signaling 56 microdeletions 56 affective disorders 56 impaired glucose tolerance 56 glomerular 56 epithelial ovarian 56 transplantation HSCT 56 CMV infections 56 GSTM1 gene 56 plasma lipid 56 Proteinuria 55 acute aortic dissection 55 malignant pancreatic 55 CFS ME 55 HGPS 55 Zollinger Ellison syndrome 55 acute leukemias 55 REM sleep behavior 55 MDM2 55 histone acetylation 55 PPCM 55 rs# [004] 55 BRAF gene 55 familial aggregation 55 asthma allergic rhinitis 55 hemolytic 55 PIK3CA 55 bladder dysfunction 55 NF kB pathway 55 Sudhir Agrawal D.Phil 55 nonmelanoma skin cancer 55 SCN5A 55 retinal degenerative disease