Related by context. All words. (Click for frequent words.) 70 pyloric stenosis 67 paraneoplastic 67 IgA deficiency 67 hereditary hemochromatosis 67 polycystic ovary syndrome PCOS 66 bladder exstrophy 66 congenital hypothyroidism 66 precocious puberty 66 polycystic ovarian syndrome PCOS 66 transfusion syndrome 66 leiomyomas 66 medium chain acyl 65 congenital disorders 65 congenital toxoplasmosis 65 adrenal function 65 IUGR 65 gestational diabetes mellitus 65 hydrops 65 hyperemesis gravidarum 65 autoimmune thyroiditis 65 choriocarcinoma 65 Heavy menstrual bleeding 65 cholestasis 65 thyrotropin 64 Phenylketonuria PKU 64 dominantly inherited 64 immunocompetent 64 Glucocorticoids 64 GH deficiency 64 epididymitis 64 Hashimoto thyroiditis 64 T1DM 64 MYH9 gene 64 molar pregnancy 64 cystic fibrosis chronic pancreatitis 64 Congenital Adrenal Hyperplasia 64 thyroid dysfunction 64 hamartoma 64 fructose intolerance 64 Sjögren syndrome 64 Neonates 64 primary ovarian insufficiency 64 de novo mutations 64 chromosome abnormality 64 Klinefelter syndrome 64 endometrial hyperplasia 64 Dysplasia 64 thyroid deficiency 64 Severe Primary IGFD 63 ADAMTS# 63 enterocolitis 63 congenital adrenal hyperplasia 63 Trichomonas vaginalis 63 genetic syndromes 63 hyperinsulinism 63 Cushing syndrome 63 hypercalciuria 63 autosomal recessive genetic 63 hemolytic disease 63 G6PD deficiency 63 ANCA associated 63 monogenic 63 Candidiasis 63 vesicoureteral reflux 63 autosomal dominant disorder 63 Hurler syndrome 63 Langerhans cell histiocytosis 63 Hypothyroidism 63 Polycystic ovary syndrome PCOS 63 Leukemias 63 hypogonadotropic hypogonadism 63 Von Willebrand disease 63 bacterial vaginosis BV 63 thrombophilia 63 vesicoureteral reflux VUR 63 Acromegaly 63 inherited mutations 63 PPCM 63 pyelonephritis 62 neurodevelopmental disorder 62 leukoencephalopathy 62 Legg Calvé Perthes disease 62 onset diabetes mellitus 62 intrapartum 62 dysgenesis 62 urolithiasis 62 bronchopulmonary dysplasia 62 leiomyoma 62 adrenal cortex 62 lichen planus 62 pulmonary hypoplasia 62 autosomal recessive disease 62 Beta thalassemia 62 Melasma 62 euthyroid 62 thyroid hormone deficiency 62 cytomegalovirus infection 62 autosomal dominant polycystic kidney 62 pulmonary hypertension PH 62 autosomal dominant 62 lymphangioleiomyomatosis LAM 62 sonographic appearance 62 chromosomal disorder 62 prepubertal 62 neoplasias 62 Endometrial cancer 62 thrombocytosis 62 Estrogen Receptor 62 chromosomal anomalies 62 proband 62 spastic diplegia 62 extramedullary 62 Gestational diabetes 62 urothelial carcinoma 62 gonadotropins 62 autoimmune thyroid 62 galactosemia 62 autosomal recessive 62 adnexal mass 62 Non Alcoholic Steatohepatitis 62 MCADD 62 myeloproliferative neoplasms 62 Genistein 62 recessive genetic 62 bronchoalveolar 62 ABCB1 62 hyperemesis 62 antiphospholipid antibodies 62 Rh factor 62 orchitis 62 metaplasia 62 Streptococcus agalactiae 62 Papillary 62 Gynecomastia 62 erythema nodosum 62 fibrosarcoma 62 bacterial prostatitis 62 ichthyosis 61 NAGS deficiency 61 Hemangiomas 61 genital abnormalities 61 Polycystic Ovary Syndrome 61 neurosensory 61 Bacterial Vaginosis 61 VUR 61 histologic subtype 61 tricuspid atresia 61 PNET 61 neuropsychiatric disorder 61 WAGR syndrome 61 SSc 61 gene MECP2 61 holoprosencephaly 61 cortical dysplasia 61 bacterium Streptococcus 61 AAT deficiency 61 idiopathic PAH 61 aneuploidies 61 pseudotumor cerebri 61 Intussusception 61 atypical hemolytic uremic syndrome 61 Interstitial cystitis 61 mtDNA mutations 61 asplenia 61 endometritis 61 intraventricular hemorrhage 61 giant cell arteritis 61 testicular germ cell 61 Bronchiolitis 61 Sclerosing 61 alpha1 antitrypsin deficiency 61 LVNC 61 varicoceles 61 LHRH receptor positive 61 dyskeratosis congenita 61 hamartomas 61 vWD 61 adrenocorticotropic hormone 61 developmental abnormalities 61 granulomatous 61 multisystem disease 61 phthalate syndrome 61 Aortic stenosis 61 myelomeningocele 61 chorioamnionitis 61 corpus luteum 61 Follicle Stimulating Hormone 61 chromosomal anomaly 61 chronic granulomatous disease 61 reproductive endocrine 61 Wilm tumor 61 IDDM 61 Hutchinson Gilford progeria 61 ambiguous genitalia 61 chromosomal aberrations 61 Hypertrophic 61 CHD7 61 von Hippel Lindau 61 Hirschsprung disease 61 Wernicke Korsakoff syndrome 61 sporadic Creutzfeldt Jakob 61 autosomal recessive disorder 61 hormonal disorder 61 Hyperplasia 61 hyperprolactinemia 61 Epstein Barr Virus EBV 61 missense mutations 61 Adrenal 61 Thromboembolism 61 polycystic ovarian syndrome 61 Cockayne syndrome 61 MCAD deficiency 61 Medulloblastoma 61 pituitary hormone 61 Placental 61 complement inhibitor eculizumab 61 behavioral disinhibition 61 Autoimmune disorders 60 dysfunctional voiding 60 mito 60 ADPKD 60 Wegener Granulomatosis 60 coagulation abnormalities 60 inhibin B 60 Bacterial vaginosis 60 mycosis fungoides 60 Hp2 2 60 prolactin levels 60 Myocarditis 60 Severe Combined Immunodeficiency 60 PCOD 60 hypothalamic amenorrhea 60 uterine tumors 60 hypophosphatasia 60 Lymphocytic 60 Dental caries 60 imperfecta 60 Polymorphic Ventricular Tachycardia CPVT 60 hay fever allergic rhinitis 60 gestational diabetes mellitus GDM 60 severe congenital neutropenia 60 polycystic ovary syndrome 60 TEL AML1 60 etiologic 60 fibroids endometriosis 60 ductal adenocarcinoma 60 vascular dysfunction 60 GPx 60 serum IGF 60 Candida infection 60 folic acid deficiency 60 CP CPPS 60 HbF 60 Chiari malformation 60 idiopathic pulmonary arterial hypertension 60 von Willebrand Disease 60 haemolytic anemia 60 Apert syndrome 60 chlamydial 60 hydronephrosis 60 renovascular hypertension 60 hemolytic 60 ductal breast cancer 60 nephrogenic 60 Respiratory Distress 60 Squamous 60 microchimerism 60 PON1 60 gastric carcinoma 60 hepatocellular carcinomas 60 Gestational 60 methicillin susceptible Staphylococcus aureus 60 Premature Ovarian Failure 60 thyroglobulin 60 hypothalamic pituitary adrenal axis 60 facial clefts 60 autoinflammatory diseases 60 adrenal insufficiency 60 hyperparathyroidism 60 neuro developmental disorders 60 cervicitis 60 polymicrobial infections 60 desmoplastic 60 NPHP 60 Prolactin 60 Dwarfism 60 Carcinoid tumors 60 familial hypercholesterolemia 60 haematologic 60 ependymoma 60 thiopurine 60 DiGeorge Syndrome 60 antiphospholipid syndrome 60 autistic regression 60 Malformations 60 Alport syndrome 60 histologic findings 60 diaper dermatitis 60 hormone human chorionic 60 bullous 60 ectodermal dysplasia 60 atresia 60 JMML 60 Adenomas 60 hepatic cirrhosis 60 Vitamin B# deficiency 60 von Willebrand disease 60 Cysts 60 thyroid stimulating hormone TSH 60 CMV infection 60 monozygotic twin 60 Sandhoff disease 60 teratoma 60 gastrointestinal dysfunction 60 endometrial biopsies 60 Morquio syndrome 60 haematopoietic 60 BCL#A 60 thyroid hormone levels 60 inherited metabolic disorders 60 CDH1 60 Growth Hormone Deficiency 60 Cryptococcus neoformans 60 CIN2 + 60 primary ciliary dyskinesia 60 idiopathic generalized epilepsy 60 Fanconi Anemia 60 PIGF 60 Lafora disease 60 vaginal cancers 60 syngeneic 60 histological subtype 60 mediastinitis 60 germline mutations 60 cardiac malformations 60 juvenile idiopathic arthritis JIA 60 interstitial cystitis IC 60 induce ovulation 60 teratogens 60 Irritable bowel syndrome IBS 60 histiocytosis 60 paragangliomas 60 Androgen 60 Leydig cell 60 Eisenmenger syndrome 60 artery stenosis 60 tuberous sclerosis complex 60 placental malaria 60 systemic amyloidosis 60 VCFS 60 Li Fraumeni syndrome 60 juvenile idiopathic arthritis 60 alpha thalassemia 60 gastric adenocarcinoma 60 anovulation 60 chromosomal defect 59 persistent pulmonary hypertension 59 gestational hypertension 59 neuritic 59 folate metabolism 59 grade squamous intraepithelial 59 recessive inheritance 59 Magnesium deficiency 59 prostate cancer CaP 59 Nonspecific 59 Acne Rosacea 59 pancytopenia 59 obliterans 59 postpartum hemorrhage 59 ASCUS 59 diabetes insipidus 59 ovarian hormones 59 IPAH 59 Brugada Syndrome 59 gallstone disease 59 Spinal muscular atrophy 59 oesophageal adenocarcinoma 59 colorectal adenoma 59 cytologic 59 FSHR 59 chromosomal disorders 59 Chlamydia trachomatis 59 microsatellite instability 59 female hormones estrogen 59 cause cardiac channelopathies 59 SGPT 59 heterozygotes 59 diabetes mellitus DM 59 hemoglobinopathies 59 growth restriction IUGR 59 pattern baldness 59 pulmonary atresia 59 Ebstein anomaly 59 RhD 59 inflammatory demyelinating 59 Histiocytosis 59 murine model 59 triiodothyronine 59 EoE 59 neurodevelopment disorder 59 immunodeficiencies 59 Chlamydia pneumoniae 59 congenital diaphragmatic hernia 59 subfertility 59 JAK mutations 59 grade cervical intraepithelial 59 PAOD 59 Hurthle cell 59 R#W [002] 59 penetrance 59 thyroiditis 59 hMG 59 carbohydrate intolerance 59 myelofibrosis polycythemia vera 59 idiopathic pulmonary 59 embryonal rhabdomyosarcoma 59 pathologic examination 59 Fatty Liver Disease 59 Polycystic Ovarian Syndrome PCOS 59 genetic neuromuscular disorder 59 invasive carcinoma 59 prematurity ROP 59 IVF ICSI 59 MECP2 gene 59 gravidarum 59 leptin deficiency 59 Hemophilia B 59 paratuberculosis 59 prostate cancer PCa 59 lactase deficiency 59 Atopic dermatitis 59 twin transfusion 59 #q# deletion 59 congenital CMV infection 59 renal cell carcinomas 59 6 phosphate dehydrogenase 59 varicocele 59 testicular tumors 59 differential gene expression 59 follicle stimulating hormone 59 Nanobacteria 59 hyperphenylalaninemia HPA due 59 inhibin 59 prenatal exposures 59 PANDAS 59 Glucocorticoid 59 chromosome deletion 59 probiotic Lactobacillus 59 channelopathies 59 secondary amenorrhea 59 recurrent UTI 59 polyarticular 59 Superoxide 59 transabdominal 59 acute GvHD 59 Phenotypic 59 puerperal psychosis 59 Heterozygous 59 hypothalamic pituitary 59 Cytogenetic 59 pancreatic insufficiency 59 Rh incompatibility 59 cerevisiae 59 situs inversus 59 cisplatin resistant 59 TPMT 59 Parkinson Disease PD 59 preserved ejection fraction 59 Nicotine dependence 59 LPS induced 59 intestinal biopsy 59 painful menstruation 59 neurogenic bladder 59 Leber congenital amaurosis 59 hypoplasia 59 Human papillomavirus HPV 59 utero exposure 59 Lichen planus 59 premenstrual syndrome PMS 59 filaggrin 59 precancerous cervical 59 cerebri 59 hepatoma 59 peripartum 59 Atopic eczema 59 metabolizing enzyme 59 pAkt 59 brachial plexus palsy 59 nulliparous 59 Wiskott Aldrich syndrome 59 alpha1 59 LH FSH 59 maternal serum 59 osteopetrosis 59 HER2 expression 59 β thalassemia 59 bronchoalveolar lavage BAL 59 MTHFR 59 hormonal abnormalities 59 hereditary deafness 59 Sezary syndrome 59 supratentorial 59 thoracic aortic aneurysm 59 benign prostatic hypertrophy BPH 59 DNA methylation patterns 59 underactive thyroid gland 59 Autistic Disorder 59 Fas ligand 59 Nonalcoholic fatty liver 59 Chronic Sinusitis 59 abnormal uterine bleeding 59 Krabbe Disease 59 primary hyperparathyroidism 59 abnormal genital 59 TTTS 59 Nonalcoholic Fatty Liver Disease 59 acute leukemias 59 Haptoglobin 59 fibrous dysplasia 59 Sydenham chorea 59 enteroviral 59 Dehydrogenase 59 fibromatosis 59 transvaginal sonography 59 Coeliac disease 59 dysmorphic features 59 Pulmonary hypertension 59 HIV HCV coinfected 59 hypothalamus pituitary 59 immunohistochemical staining 59 Pelvic Inflammatory Disease 59 bronchoalveolar lavage 59 atrophic gastritis 59 HeFH 59 Juvenile Idiopathic Arthritis 59 lymphocyte proliferation 59 premenstrual dysphoric disorder PMDD 59 demyelinating 59 Retinoblastoma 59 CYP#C# [002] 59 simplex virus 59 congenital deafness 59 gonadotrophin 59 lactose malabsorption 59 nonischemic 59 Clusterin 59 carcinoid tumor 59 homozygosity 59 intracerebral 59 Chronic lymphocytic leukemia 59 idiopathic intracranial hypertension 58 HER2 overexpression 58 subependymal giant cell 58 bronchopulmonary dysplasia BPD 58 fetal echocardiogram 58 generalized epilepsy 58 prenatally diagnosed 58 Peptide YY 58 Bacteremia 58 apolipoprotein E gene 58 Hypospadias 58 septo optic dysplasia 58 Menkes disease 58 human leukocyte antigen HLA 58 mitral stenosis 58 glutamic acid decarboxylase 58 pancreatic endocrine 58 antidiuretic hormone 58 hereditary hemorrhagic telangiectasia 58 toxemia 58 Idiopathic 58 HNPCC 58 phenylketonuria PKU 58 Henoch purpura 58 Venous thromboembolism 58 hyperinsulinemia 58 hepatorenal syndrome 58 Neurogenesis 58 autoimmune hemolytic anemia 58 treat benign prostatic 58 thromboembolic disease 58 metabolizer 58 Proteinuria 58 Leber Congenital Amaurosis LCA 58 Hyperthyroidism 58 GSTT1 58 HepG2 cells 58 alveolar epithelial cells 58 bacteriuria 58 multivariate Cox 58 potentially modifiable 58 C1q 58 Elevated serum 58 STK# gene 58 Sanfilippo Syndrome 58 lysosomal storage disorder 58 LRP5 58 antithyroid 58 Polycythemia 58 Papillomavirus 58 progressive neurodegenerative disorder 58 Prehypertension 58 Chronic sinusitis 58 enteropathy 58 AST ALT 58 limb deformities 58 polycystic ovarian disease 58 tumoral 58 Genetic predisposition 58 motor neuron degeneration 58 Benign prostatic hyperplasia 58 atypical hyperplasia 58 Osteogenesis Imperfecta 58 ptau 58 PTLD 58 Insulin sensitivity 58 autoimmune pancreatitis 58 hypovitaminosis D 58 chronic myeloid 58 airway reactivity 58 medulloblastoma malignant brain tumor 58 N. gonorrhoeae 58 sonographic diagnosis 58 moyamoya 58 rotaviruses 58 Irritable bowel syndrome 58 Polycystic Ovary Syndrome PCOS 58 Cockayne Syndrome 58 transgenic mouse models 58 lymphoproliferative disease 58 mixed hyperlipidemia 58 chlamydial infection 58 #q#.# [001] 58 metastatic neuroendocrine tumors 58 ovulation induction 58 Neisseria gonorrhoeae 58 isoprostane 58 MELAS 58 pT2 58 mammary gland tumors 58 ceroid lipofuscinosis NCL 58 Mycoplasma pneumoniae 58 Churg Strauss syndrome 58 squamous intraepithelial lesions 58 neonatal morbidity 58 inherited retinal degeneration 58 Histologic 58 airway hyperresponsiveness 58 GISTs 58 discoid lupus 58 vitamin B# folic acid 58 uterus didelphys 58 pheochromocytoma 58 immunodeficiency 58 Hemochromatosis 58 phenotypic expression 58 metastatic malignant 58 Iron Deficiency 58 dehydrogenase deficiency 58 reproductive abnormalities 58 recessive trait 58 hepatoblastoma 58 late onset hypogonadism 58 Zollinger Ellison syndrome 58 KCNE2 58 thyroid stimulating hormone 58 preeclamptic women 58 Polycystic ovary syndrome 58 preterm neonates 58 myopathies 58 murine leukemia virus 58 Amino acid 58 methemoglobinemia 58 coagulopathy 58 HLA DQ2 58 FXTAS 58 endocrine disorder 58 VCUG 58 Phenylketonuria 58 Adrenal Fatigue 58 pregnancy bacterial vaginosis 58 vaginal flora 58 gastrointestinal stromal tumors GISTs 58 myometrium 58 craniofacial abnormalities 58 Urinary tract 58 lysosomal storage disease 58 chromosome #q#.# [001] 58 essential thrombocythemia 58 Trichophyton rubrum 58 vWF 58 hypercholesterolaemia 58 tumorigenicity 58 chronic lymphocytic 58 familial aggregation 58 Cytomegalovirus CMV 58 familial adenomatous polyposis 58 periventricular leukomalacia 58 Hurler Syndrome 58 tuberculous 58 maternally derived 58 coinfection 58 Adiponectin 58 pre eclamptic 58 #q# deletion syndrome 58 Hereditary angioedema 58 hypoxic ischemic encephalopathy 58 nonsense mutation 58 dopamine receptor gene 58 Catheter Associated 58 DiGeorge syndrome rare 58 Anaemia 58 Neurofibromatosis Type 58 FMR1 58 Retinopathy 58 Abdominal ultrasound 58 Thiazolidinediones 58 Mucopolysaccharidosis 58 multivitamin supplementation 58 bacterium Listeria 58 Genetic Variation 58 Iron deficiency anemia 58 fetal fibronectin 58 NSCLC tumors 58 immunoreactivity 58 allogeneic HSCT 58 SIADH 58 Holoprosencephaly 58 #q#.# deletion syndrome 58 Systemic lupus erythematosus 58 lupus anticoagulant 58 immunodeficiency disorder 58 Neural Tube Defects 58 Erythema 58 comorbid anxiety 58 recurrent miscarriage 58 Chiari Malformation 58 hemodilution 58 BMPR2 58 Peutz Jeghers syndrome 58 narcolepsy cataplexy 58 serum leptin 58 C. trachomatis 58 PCNSL 58 primary aldosteronism 58 HELLP syndrome 58 mutated K ras 58 BPS IC 58 infantile hemangioma 58 irregular menses 58 fetal aneuploidy 58 atopic eczema 58 renal tubular 58 nondemented 58 Fatty acid 58 homocystinuria 58 tract infections 58 Polymorphisms 58 Morquio 58 metabolic abnormality 58 astrocytomas 58 hereditary predisposition 58 antibody titer 58 NF1 58 lipid elevations 58 RIP1 58 exocrine 58 activin 58 Hereditary angioedema HAE 58 Metastases 58 neurofibromas 58 cranial irradiation 58 lymphoblasts 58 Human papillomavirus 58 polymyalgia rheumatica 58 Glomerular 58 CHDs 58 P. falciparum malaria 58 Becker muscular dystrophy 58 ataxia telangiectasia 58 Trichomonas 58 glomerulonephritis 58 hepatic liver 58 subclinical hypothyroidism 57 paraganglioma 57 murine models 57 post transplant lymphoproliferative 57 cryptorchidism 57 hypereosinophilic syndrome 57 Systemic lupus erythematosus SLE 57 dysmotility 57 COPEGUS therapy 57 arachidonic acid AA 57 androgen excess 57 prostate carcinoma 57 karyotypes 57 trophoblastic 57 HHV 6 57 SOD2 gene 57 haemochromatosis 57 Joubert syndrome 57 spinocerebellar ataxia 57 Thromboembolic 57 Leber congenital amaurosis LCA 57 DiGeorge syndrome 57 mitochondrial mutations 57 subclinical atherosclerosis 57 MeCP2 gene 57 ovulatory cycles 57 Angiotensin II 57 NOMID 57 neurological abnormalities 57 herpesviruses 57 myositis 57 transcranial Doppler ultrasound 57 steroidogenesis 57 SNHL 57 intraepithelial neoplasia 57 renal allograft 57 interleukin IL -# 57 Spasticity 57 monoclonal gammopathy 57 myofascial pain syndrome 57 Ribavirin causes 57 mastocytosis 57 ERK signaling 57 Acute Myeloid Leukaemia AML 57 adenomyosis 57 Leber Hereditary Optic Neuropathy 57 Familial hypercholesterolemia 57 apolipoprotein E4 57 HLA DR4 57 mosaicism 57 proliferative retinopathy 57 congenital cataract 57 gonadal 57 congential 57 Bronchiectasis 57 Hip dysplasia 57 peritoneal fluid 57 cervical intraepithelial neoplasia 57 Periodontitis 57 severe hyperbilirubinemia 57 hyperplastic 57 Immune Responses 57 1 diabetes T1D 57 aminotransferase 57 atypical ductal hyperplasia 57 thrombocytopenia neutropenia 57 congenital deficiency 57 airway responsiveness 57 Testicular 57 myeloproliferative 57 biliary atresia rare 57 congenital anomalies 57 CC genotype 57 familial hypercholesterolemia FH 57 dysglycemia 57 epithelial ovarian cancer 57 Hypoglycaemia 57 Hyperkalemia 57 allelic variants 57 mucins 57 monozygotic 57 collagenous colitis 57 PB1 F2 57 Helicobacter pylori infection 57 Valvular 57 imatinib resistance 57 VLBW 57 atopic disease 57 Upregulation 57 K ras mutations 57 hyperandrogenism 57 Comorbidities 57 bicuspid valve 57 microdeletion 57 Rheumatoid 57 neurodevelopmental outcome 57 Brugada syndrome 57 viral etiology 57 juvenile myelomonocytic leukemia 57 Oncogenic 57 overactive bladder symptoms 57 renal fibrosis 57 candidemia 57 ectopic expression 57 acute myeloid 57 amenorrhoea 57 abnormal vaginal bleeding 57 chromosomal rearrangement 57 Wilms Tumor 57 neural tube defect 57 iduronate 2 57 folate concentrations 57 Bronchopulmonary Dysplasia 57 hirsutism 57 Heritability 57 NOD mouse 57 Prostaglandins 57 chromosome #q#.# [002] 57 xeroderma pigmentosum 57 pernicious anemia 57 hematological parameters 57 Atopic 57 myomas 57 Epstein Barr virus EBV 57 Arrhythmogenic Right Ventricular Cardiomyopathy 57 serologically 57 monocytic 57 Secondary Hyperparathyroidism 57 sCJD 57 prolapsed uterus 57 VEGF expression 57 lysophosphatidic acid 57 BH4 deficiency 57 levonorgestrel releasing 57 conductance regulator 57 congenital disorder 57 Male Pattern Baldness 57 eNOS 57 chorionic villi 57 neurodevelopmental disability 57 Klotho gene 57 placenta praevia 57 azoospermia 57 periventricular 57 celiac sprue 57 hypertrophic cardiomyopathy HCM 57 Uterine fibroids 57 posterior urethral valves 57 colorectal cancer CRC 57 aetiological 57 overt hypothyroidism 57 LRAT 57 Epstein Barr Virus 57 hyperalgesia 57 Von Willebrand 57 Ferritin 57 Prolapse 57 uterus fallopian tubes 57 Valproate 57 advanced adenoma 57 Lipodystrophy 57 MGUS 57 intestinal permeability 57 elevated serum ALT 57 erythropoietic 57 Lymphoid 57 Dystrophin 57 Sjogren Syndrome 57 steroid dexamethasone 57 untreated celiac disease 57 TGF ß 57 cytomegalovirus CMV 57 Acute Bacterial Sinusitis ABS 57 endocrine tumors 57 hyper IgE syndrome 57 HGPIN 57 TCF#L# gene 57 HIV seropositive 57 hyperpyrexia 57 Cowden syndrome 57 Chemotherapy induced 57 paroxysmal nocturnal hemoglobinuria 57 Thrombocytopenia 57 rare chromosomal disorder 57 LQTS 57 Crigler Najjar syndrome 57 PTPN# 57 metabolic acidosis 57 Fibrosis 57 polyhydramnios 57 colorectal carcinoma 57 Fragile X Syndrome 57 Human Papilloma Virus 57 nonbacterial prostatitis 57 APOE genotype 57 LNG IUS 57 myeloproliferative diseases 57 alpha hydroxyprogesterone caproate 57 congenital blindness 57 oral clefts 57 Monocyte 57 abacavir Ziagen 57 eosinophilic 57 atopy 57 pituitary adenomas 57 bronchial hyperresponsiveness 57 associated tremor ataxia 57 syndrome FAS 57 Hypothalamic 57 hyperammonemia 57 Acidosis 57 Ankylosing spondylitis 57 systemic lupus erythematosus SLE 57 maternally inherited 57 Ectopia Cordis 57 intersexuality