Related by context. All words. (Click for frequent words.) 68 dominantly inherited 67 holoprosencephaly 65 sporadic Creutzfeldt Jakob 65 inflammatory demyelinating 65 autosomal recessive genetic 65 Nonalcoholic fatty liver 64 autosomal recessive 64 1 diabetes T1D 64 Niemann Pick disease 63 myeloproliferative neoplasms MPNs 63 autosomal dominant polycystic kidney 63 ANCA associated 63 Hutchinson Gilford progeria 63 collagen vascular 63 Spinal muscular atrophy 63 etiologic agent 63 autosomal recessive disease 63 Myasthenia gravis 63 progressive neurodegenerative 63 autosomal recessive disorder 63 von Hippel Lindau 63 gene MECP2 63 Tuberous sclerosis 63 NPHP 62 Celiac sprue 62 Anaplasmosis 62 gastrointestinal dysfunction 62 Osteogenesis imperfecta 62 Systemic lupus erythematosus SLE 62 cystic fibrosis chronic pancreatitis 62 imperfecta 62 immunodeficiencies 62 Medulloblastoma 62 Fatty liver 62 progressive neurodegenerative disorder 62 autosomal dominant disorder 62 Chronic lymphocytic leukemia 62 TTR amyloidosis 62 Kufs disease 62 chronic myeloid 62 Pervasive Developmental Disorders 62 malayi 62 hereditary spastic paraplegia 62 HHV 6 62 Myocarditis 61 G6PD deficiency 61 hemorrhagic colitis 61 transmissible spongiform encephalopathies 61 leukemia lymphomas 61 hypereosinophilic syndrome 61 genetic lysosomal storage 61 nonhereditary 61 chronic rheumatic 61 Von Hippel Lindau 61 Moraxella bovis 61 hereditary hemochromatosis 61 Acute Bacterial Sinusitis ABS 61 inherited retinal 61 Sjogren Syndrome 61 incurable degenerative 61 Primary immunodeficiency 61 Neisseria meningitides 61 congenital disorders 61 neuro degenerative 61 Fetal alcohol 61 Beta thalassemia 61 CDH1 61 diabetes mellitus DM 61 MELAS 61 Brugada Syndrome 61 B streptococcal 61 germline mutations 61 leptin deficiency 61 Crigler Najjar syndrome 61 NOMID 61 fibrosarcoma 61 Myotonic dystrophy 61 hereditary predisposition 61 P. ovale 61 chronic obstructive airway 61 neuro developmental disorders 61 sickle cell cystic fibrosis 61 Henoch purpura 61 recessive genetic 61 MYH9 gene 61 Magnesium deficiency 61 systemic autoimmune 61 cutaneous lupus 61 renal failure interstitial lung 60 Tay Sachs thalassemia 60 Fanconi anemia FA 60 Lymphocytic 60 myeloproliferative 60 monogenic 60 neuropsychiatric disorder 60 Iron deficiency anemia 60 autoimmune thyroiditis 60 fatal neurodegenerative 60 immunodeficiency disorder 60 mammary gland tumors 60 multisystem disease 60 Lewy Body 60 Hereditary angioedema 60 erythema nodosum 60 rare autosomal recessive 60 Childhood Disorder 60 XMRV retrovirus 60 chronic lymphocytic 60 Mucopolysaccharidosis 60 juvenile myelomonocytic leukemia 60 neurofibromatosis type 60 Severe Combined Immunodeficiency 60 MPGN 60 chronic autoimmune disorder 60 LHON 60 Usher Syndrome 60 nonbacterial prostatitis 60 Bronchiectasis 60 Alport syndrome 60 VCFS 60 hemophagocytic lymphohistiocytosis 60 post transplant lymphoproliferative 60 Neurofibromatosis Type 60 Usher syndrome 60 Hereditary angioedema HAE 60 erythematosus 60 deafness neurological 60 Ribavirin causes 60 neuritic 60 Meckel Gruber 60 Streptococcus agalactiae 60 Li Fraumeni syndrome 60 enterocolitis 60 Entamoeba histolytica 60 multiple sclerosis epilepsy 60 parainfluenza virus 60 Leukemias 60 Neimann Pick 60 Lichen planus 60 chromosome #q#.# [001] 59 Bordetella pertussis 59 polycythemia vera PV 59 Acute myeloid leukemia 59 Bronchopulmonary Dysplasia 59 bacterium Mycobacterium tuberculosis 59 metastatic gastric 59 neurodegenerative disorder characterized 59 myasthenia gravis neuromuscular 59 alpha1 antitrypsin deficiency 59 polymyalgia rheumatica 59 Chlamydia psittaci 59 Porcine circovirus 59 discoid lupus 59 nephronophthisis 59 Bullous 59 aniridia 59 progressive degenerative neurological 59 rheumatoid arthritis osteoarthritis ankylosing 59 lichen planus 59 ataxias 59 progranulin mutations 59 motor neuron diseases 59 Arrhythmogenic Right Ventricular Cardiomyopathy 59 Neisseria 59 PNET 59 leukodystrophies 59 idiopathic thrombocytopenic purpura 59 tricuspid atresia 59 roseola 59 paraneoplastic 59 clinically heterogeneous 59 Cytomegalovirus CMV 59 Lyme borreliosis 59 vaginal candidiasis 59 cause cardiac channelopathies 59 retrovirus XMRV 59 Acute Renal Failure 59 autoinflammatory 59 Juvenile Idiopathic Arthritis JIA 59 neurological manifestations 59 kidney urologic 59 cysticercosis 59 Trichomonas vaginalis 59 immuno deficiency 59 genetic syndromes 59 Becker muscular dystrophy 59 multiple sclerosis psoriasis 59 cystic fibrosis Duchenne muscular 59 aMCI precursor 59 Hypertensive heart 59 Leptospira 59 Candidiasis 59 Sanfilippo Syndrome 59 dyskeratosis congenita 59 Pelvic Inflammatory Disease 59 SSc 59 rheumatoid arthritis inflammatory bowel 59 gastric carcinoma 59 simplex virus 59 serologically 59 Waldenstrom macroglobulinemia 59 β thalassemia 59 Escherichia coli Klebsiella pneumoniae 59 twin transfusion 59 Ehrlichia 59 childhood disintegrative disorder 59 Hypophosphatasia 59 muscular dystrophy cystic fibrosis 59 Ectodermal Dysplasia 59 Noonan Syndrome 59 spinal muscular atrophy SMA 59 Atopic dermatitis 59 Dilated cardiomyopathy 59 NASH Huntington 59 inherited neurodegenerative 59 Visceral leishmaniasis 59 Anaplasma 59 Creutzfeldt Jacob 59 Cockayne syndrome 59 diabetes dyslipidemia 59 Pneumococcal pneumonia 59 GPC5 59 vWD 58 typhi 58 IgA deficiency 58 Cryptococcus neoformans 58 Balamuthia 58 Systemic lupus erythematosus 58 maple syrup urine 58 sCJD 58 molecular etiology 58 neurodevelopment disorder 58 Acidosis 58 PKU genetic 58 de novo mutations 58 neurological disorder affecting 58 systemic mastocytosis 58 velo cardio facial 58 myotonic muscular dystrophy 58 astrocytomas 58 dysgenesis 58 Interstitial cystitis 58 cardiovascular restenosis cancer 58 TCF#L# gene 58 Pelvic inflammatory 58 spinocerebellar ataxia type 58 severe congenital neutropenia 58 Leber Congenital Amaurosis LCA 58 Acute Respiratory Failure 58 MCAD deficiency 58 Ectopia Cordis 58 Ischemic heart 58 psoriasis psoriatic arthritis 58 Polyneuropathy 58 Multidrug resistant 58 Glioblastoma Multiforme GBM 58 hereditary hemorrhagic telangiectasia 58 Genetic variants 58 antiphospholipid syndrome 58 serovar 58 Epidermolysis bullosa 58 myeloproliferative neoplasms 58 Hurler syndrome 58 Hip dysplasia 58 Chronic Lung 58 CHARGE syndrome 58 Myelodysplastic syndrome 58 Sezary syndrome 58 Pelizaeus Merzbacher disease 58 molybdenum cofactor deficiency 58 #q#.# deletion syndrome 58 plaque buildup restricts 58 familial dysautonomia 58 Polycythemia vera 58 herpes zoster shingles 58 fibrosing 58 mycobacterial infection 58 Leber congenital amaurosis 58 mastocytosis 58 babesia 58 Neurofibromatosis type 58 herpes encephalitis 58 cryptogenic 58 tuberous sclerosis complex 58 cystic kidney 58 otitis externa 58 neurological disorders orphan 58 Bardet Biedl syndrome 58 pulmonary hypertension PH 58 fronto temporal dementia 58 glutamic acid decarboxylase 58 N. meningitidis 58 transthyretin amyloidosis 58 transfusion syndrome 58 transmissible spongiform encephalopathies TSEs 58 thrombophilia 58 Citrobacter 58 phthalate syndrome 58 susceptibility gene 58 CHD7 58 autosomal dominant 58 Polycystic ovary syndrome 58 diabetic kidney 58 Tuberous Sclerosis Complex 58 Vitamin D insufficiency 58 C. trachomatis 58 neuro degenerative disease 58 Irritable bowel syndrome IBS 58 Respiratory syncytial virus RSV 58 Hashimoto thyroiditis 58 JAK mutations 58 primary ciliary dyskinesia 58 bacteria Neisseria meningitidis 58 Genetic mutation 58 rotaviruses 58 Endometrial cancer 58 congenital toxoplasmosis 58 Moraxella catarrhalis 58 Lymphatic filariasis 58 #p#.# [001] 58 systemic amyloidosis 58 Alport Syndrome 58 Eosinophilic 58 Lepto 58 syngeneic 58 Moyamoya 58 Epstein Barr Virus EBV 58 membranous nephritis 58 Von Willebrand disease 58 Creutzfeld Jakob disease 58 Idiopathic 58 Inflammatory bowel diseases 58 metastatic neuroendocrine tumors 58 immune thrombocytopenic purpura 58 recessive dystrophic epidermolysis bullosa 58 Aplastic anemia 58 Arthrogryposis Multiplex 58 flavivirus 58 chromosome abnormality 58 Niemann Pick type 58 dermatitis herpetiformis 58 Mycoplasma pneumoniae 58 Sporadic CJD 58 airway hyperresponsiveness 58 hydatid disease 58 Guillain Barr 58 progressive retinal degenerative 57 Tay Sachs Disease 57 microchimerism 57 autistic enterocolitis 57 Herpes zoster 57 AAT Deficiency 57 renal hepatic 57 herpesviruses 57 dystrophies 57 respiratory syndrome virus 57 Hurthle cell 57 limb girdle muscular dystrophy 57 hereditary deafness 57 congenital deficiency 57 thalassemia sickle cell 57 Ischaemic heart 57 constipation predominant irritable bowel 57 predisposing factor 57 Chemotherapy induced 57 Invasive pneumococcal disease 57 autoimmune uveitis 57 cytomegalovirus infection 57 ichthyosis vulgaris 57 autoimmune hemolytic anemia 57 spongiform encephalopathies 57 Jakob Disease 57 multi factorial disease 57 varicella infection 57 hypercholesterolemia liver 57 Lou Gehrigs disease 57 medium chain acyl 57 Human papillomavirus 57 degenerative neurological diseases 57 Muscular dystrophy 57 ectodermal dysplasia 57 sarcoid 57 muscular dystrophy cerebral palsy 57 bacterium Streptococcus pneumoniae 57 treating sarcoma testicular 57 Congenital heart 57 rheumatic disorders 57 Herpes Simplex Virus 57 Zinc deficiency 57 susceptibility loci 57 Trichophyton rubrum 57 mosaicism 57 KRAS oncogene 57 Lysosomal storage 57 Hemorrhagic 57 Wiskott Aldrich syndrome 57 bovis 57 ADA SCID 57 Meningiomas 57 hereditary degenerative 57 retinal dysfunction 57 HGPS 57 neurodevelopmental disorder characterized 57 Polycystic kidney disease 57 Uncontrolled hypertension 57 neurona 57 Ciguatera 57 Duchene muscular dystrophy 57 Morquio syndrome 57 nonhuman primate model 57 ataxia telangiectasia 57 epilepsy multiple sclerosis 57 HMPV 57 chlamydial 57 Graft Versus Host 57 autoimmune disorders asthma 57 multifactorial disease 57 Streptococcus equi 57 rheumatoid arthritis systemic lupus 57 African trypanosomiasis 57 neuro degenerative disorders 57 Li Fraumeni 57 Myeloproliferative 57 debilitating neurodegenerative disorder 57 nephrosis 57 asymptomatic carriers 57 progressive multifocal PML 57 abnormal hemoglobin 57 optic atrophy 57 Chronic Obstructive Pulmonary 57 Lafora disease 57 HIV coinfected 57 paraganglioma 57 protozoan parasite 57 galactosemia 57 facioscapulohumeral muscular dystrophy 57 inherited predisposition 57 hemolytic anemia 57 melanocortin receptor 57 coccidia 57 atypical scrapie 57 MECP2 gene 57 Hemochromatosis 57 chromosome #q#.# deletion 57 Parathyroid 57 Peripheral artery 57 embryonal rhabdomyosarcoma 57 Dysplasia 57 papillary renal cell carcinoma 57 autoinflammatory diseases 57 immunocompetent 57 neuro developmental disorder 57 developmental abnormalities 57 potent inducer 57 Major depressive disorder 57 syndromic 57 meningitis septicemia 57 epiglottitis 57 oncogenic HPV 57 Pasteurella 57 Circovirus 57 neoplasias 57 Tick borne 57 PANDAS 57 Urinary tract 57 familial polyposis 57 demyelinating 57 Gastro intestinal 57 chorioamnionitis 57 Aeromonas 57 flaviviruses 57 myelogenous leukemia 57 aciduria 57 lysosomal storage disease 57 included exfoliative dermatitis 57 hemorrhagic cystitis 57 LRP5 57 Opportunistic infections 57 complement inhibitor eculizumab 57 Opioid induced bowel dysfunction 57 #q#.# [001] 57 allergic airway 57 multisystem disorder 57 clefting 57 primary hyperparathyroidism 57 LVNC 57 lateral sclerosis ALS 57 auditory neuropathy 57 Pulmonary arterial hypertension 57 human metapneumovirus 57 chronic granulomatous disease 57 Enterobacter cloacae 57 hemolytic disease 57 Fibromyalgia syndrome 57 Transmissible 57 disorder Creutzfeldt Jakob 57 pyogenes 57 incurable degenerative brain 57 systemic juvenile idiopathic 57 Vitamin B# deficiency 57 congenital insensitivity 57 spontaneous miscarriages 57 Babesia 57 Niemann Pick 57 Borrelia 57 Dravet syndrome 57 arboviral 57 neurogenic bladder 57 myalgic encephalomyelitis 57 Ehrlichiosis 57 Proteus syndrome 57 Peripheral artery disease 57 chlamydiosis 57 familial adenomatous polyposis FAP 57 histologically active 57 rheumatoid arthritis lupus 57 mitochondrial disorders 56 monozygotic twin 56 epilepsy Parkinson disease 56 Cystic fibrosis CF 56 Congenital Adrenal Hyperplasia 56 immunodeficiency 56 Lymphoid 56 Dengue Shock 56 Histoplasmosis 56 simian foamy virus 56 leiomyomas 56 Parvovirus B# 56 myelofibrosis polycythemia vera 56 encephalomyelitis 56 abnormal genital 56 parainfluenza 56 Tourette Syndrome TS 56 humans variant Creutzfeldt 56 Variant CJD 56 variant Creutzfeldt Jacob 56 JAK2 enzyme 56 spastic diplegia 56 variable immunodeficiency 56 idiopathic generalized epilepsy 56 Sjögren syndrome 56 bacterium Neisseria meningitidis 56 AAT deficiency 56 Bartonella henselae 56 neurocysticercosis 56 Lennox Gastaut syndrome 56 swine vesicular 56 Wiskott Aldrich Syndrome 56 hypovitaminosis D 56 Wegener granulomatosis 56 Epstein Barr virus EBV 56 Diabetic neuropathy 56 Rheumatoid 56 ARVD 56 chromosomal anomaly 56 contagious bacterial 56 Muscular dystrophies 56 heritable diseases 56 Herpes simplex virus 56 Hemolytic Uremic Syndrome 56 myalgic encephalomyelitis ME 56 aphthous stomatitis 56 Cockayne Syndrome 56 hypokalemia hypomagnesemia 56 Prion diseases 56 neisseria 56 primary dysmenorrhea 56 Leber congenital amaurosis LCA 56 enteroviruses 56 Genetic predisposition 56 Myelodysplastic syndromes 56 Squamous Cell 56 Pulmonary hypertension 56 murine leukemia virus 56 parasiticus 56 Canavan Disease 56 Viral infections 56 feline calicivirus 56 microdeletions 56 severe malignant osteopetrosis 56 B. henselae 56 seropositivity 56 alpha1 antitrypsin AAT deficiency 56 oligodendrogliomas 56 rheumatoid arthritis gout 56 Acute otitis media 56 pneumonia septicemia 56 Morquio Syndrome 56 CCR5 delta# 56 Squamous 56 hereditary disorders 56 Kleine Levin 56 paroxysmal nocturnal hemoglobinuria 56 apolipoprotein E gene 56 subependymal giant cell 56 Familial hypercholesterolemia 56 Flavivirus 56 Duchenne muscular dystrophy DMD 56 IPAH 56 mycobacterium avium 56 Irritable bowel syndrome 56 associated tremor ataxia 56 Acute Leukemia 56 lymphocytic choriomeningitis virus LCMV 56 myopathies 56 vivax 56 herpes zoster virus 56 Pemphigus 56 Hookworm 56 haemolytic uraemic syndrome 56 WDR# 56 streptococcus pneumonia 56 polymicrobial infections 56 basal cell nevus syndrome 56 channelopathies 56 neurobehavioral disorders 56 maternally inherited 56 Endocarditis 56 Trypanosoma 56 progranulin gene 56 metaplasia 56 Acute Myelogenous Leukemia 56 Polymorphisms 56 Phenylketonuria PKU 56 Severe Primary IGFD 56 common disabling neurological 56 Cerebral malaria 56 meningitis encephalitis 56 Parkinson degenerative 56 Babesiosis 56 Philadelphia Chromosome Positive 56 gene polymorphism 56 progressive neuromuscular 56 uterus didelphys 56 Krabbe Disease 56 transmissible spongiform encephalopathy 56 polycythemia vera essential thrombocythemia 56 Bronchiolitis 56 Infant botulism 56 Basal Cell 56 genus Plasmodium 56 rheumatologic 56 Trichophyton 56 histiocytosis 56 mycosis fungoides 56 typhimurium 56 myocardial infarction ventricular fibrillation 56 polycystic 56 fatal neurodegenerative disorder 56 Legg Calvé Perthes disease 56 lymphocytic leukemia 56 hepatoblastoma 56 primary immunodeficiencies 56 myotonia 56 developing Surfactant Therapies 56 Adenoviral 56 Chronic wasting 56 nontuberculous mycobacteria 56 Creutzfeld Jakob Disease 56 Hemangiomas 56 congenital deafness 56 autoimmune thyroid 56 Pompe Disease 56 treat musculoskeletal metabolic 56 retinitis pigmentosa degenerative 56 motor neuron degeneration 56 Epstein Barr Virus 56 refractory Hodgkin 56 HLA DRB1 * 56 acute lymphoid leukemia 56 Hypertrophic 56 genital lesions 56 Single Nucleotide Polymorphisms SNPs 56 HLA DR4 56 xeroderma pigmentosum 56 Leber Hereditary Optic Neuropathy 56 mutated K ras 56 cortical dysplasia 56 coinfection 56 Wolf Hirschhorn 56 distemper virus 56 ADPKD 56 Trichomonas 56 lupus scleroderma 56 essential thrombocythemia ET 56 Motor neurone disease 56 orthopoxvirus 56 Thyroid nodules 56 Haptoglobin 56 narcolepsy cataplexy 56 human immunodeficiency 56 polycystic kidneys 56 chronic renal disease 56 recessive inheritance 56 Phenylketonuria 56 CMV infections 56 Diabetes mellitus 56 diagnose coronary artery 56 HYPP 56 Hypospadias 56 sporadic ALS 56 inherited neurological disorder 56 Hemolytic uremic syndrome 56 gastroesophageal reflux GERD 56 Actinic Keratosis 56 pathological hallmarks 56 Intravenous immunoglobulin 56 Pancreatic insufficiency 56 polyarticular 56 indications Dupuytren 56 Hyperthyroidism 56 comorbid anxiety 56 microdeletion 56 giant cell arteritis 56 metastatic malignant 56 immunodeficient 56 Cellulitis 56 mental retardation blindness 56 heterotaxy 56 genes predisposing 56 Coronaviruses 56 chronic inflammatory bowel 56 influenzae 56 contagious viral infection 56 opsoclonus myoclonus syndrome 56 Radiographic findings 56 lymphoproliferative disorders 56 rare chromosomal disorder 56 recessive trait 56 squamous cell lung cancer 56 multivessel coronary artery 56 causative mutations 56 CC genotype 56 neuronal ceroid lipofuscinosis 56 single celled parasite 56 Meckel Gruber syndrome 56 Trypanosoma brucei 56 Apolipoprotein E 56 inherited mutations 56 Retinitis Pigmentosa RP 56 bacteraemia 56 varicella chickenpox 56 enteroviral 56 congenital adrenal hyperplasia CAH 56 #q# deletion 56 Polycystic ovary syndrome PCOS 56 Porphyria 56 Dental caries 56 cholestasis 56 SOD2 gene 56 Maven Semantic 55 A. fumigatus 55 ceroid lipofuscinosis NCL 55 Rotavirus infection 55 MELAS syndrome 55 prenatally diagnosed 55 glomerulonephritis 55 idiopathic pulmonary arterial hypertension 55 Eisenmenger syndrome 55 Respiratory Syncytial Virus 55 hemoglobinopathies 55 Sickle cell 55 hypothalamic amenorrhea 55 Bacterial vaginosis 55 neurogenetic 55 Diffuse Intrinsic Pontine Glioma 55 monoclonal gammopathy 55 multiple sclerosis lupus 55 convulsive disorders 55 hay fever allergic rhinitis 55 FMR1 gene 55 hereditary pancreatitis 55 LRAT 55 arteritis 55 pheochromocytoma 55 arterial calcification 55 curing muscular dystrophy 55 Hp2 2 55 Gestational diabetes 55 myeloproliferative disorders 55 Francisella 55 HELLP 55 Onchocerca volvulus 55 chromosomal anomalies 55 Benign prostatic hyperplasia 55 myasthenia gravis MG 55 type 1diabetes 55 6 phosphate dehydrogenase 55 neonatal respiratory distress 55 MGUS 55 BRSV 55 psoriasis Crohn disease 55 Ulcerative colitis 55 Staphylococcal 55 Folic acid deficiency 55 lysosomal storage diseases 55 naturally occurring bacterium 55 meningitides 55 Streptococcus pneumonia 55 Ebola Hemorrhagic Fever 55 cytogenetic abnormalities 55 hypertension cardiovascular disease 55 lymphoproliferative disease 55 Alleles 55 Feline leukemia 55 invasive fungal 55 methicillin susceptible Staphylococcus aureus 55 primary immunodeficiency 55 extramedullary 55 contagious bacterial infection 55 Hemophilia B 55 Sandhoff disease 55 skeletal dysplasia 55 Pleural Mesothelioma 55 granulosa cell 55 Eosinophilic esophagitis 55 spinal muscle atrophy 55 hypophosphatasia 55 bronchogenic carcinoma 55 APOL1 55 Variant Creutzfeldt Jakob Disease 55 demyelinating disease 55 phenotypic expression 55 lacunar 55 arthritis lupus 55 vesicular stomatitis virus 55 Smith Lemli Opitz syndrome 55 Variant Creutzfeldt Jakob 55 herpes viruses 55 renal kidney 55 Canine influenza 55 atopic disorders 55 Psoriatic arthritis 55 incurable genetic 55 neuropathic pain spasticity 55 noncontagious disease 55 cystic fibrosis sickle cell 55 RMSF 55 chronic idiopathic urticaria 55 GBA mutations 55 FXTAS 55 nonbacterial 55 dermatomyositis 55 bacteremic pneumonia 55 von Willebrand disease 55 Acromegaly 55 testicular germ cell 55 cystic fibrosis muscular dystrophy 55 HLA identical 55 HLA DRB1 55 polymyalgia 55 missense mutations 55 Retinitis pigmentosa 55 Stargardt Macular Dystrophy 55 cisplatin resistant 55 Thorough cooking kills 55 Respiratory Syncytial Virus RSV 55 pyelonephritis 55 hypertension hypercholesterolemia 55 Hypertrophic cardiomyopathy 55 Brugada syndrome 55 Acute lymphoblastic leukemia 55 cell acute lymphoblastic 55 smoldering myeloma 55 Gastroparesis 55 Metastases 55 hypogonadotropic hypogonadism 55 gastrointestinal stromal tumors GISTs 55 Adrenoleukodystrophy 55 Salmonella Campylobacter 55 Autoantibodies 55 Gorlin syndrome 55 esophageal reflux 55 gonococcal 55 idiopathic PAH 55 Keratitis 55 multiple sclerosis inflammatory bowel 55 lupus multiple sclerosis 55 chromosome #p#.# 55 diffuse intrinsic pontine glioma 55 anogenital warts 55 causative genes 55 parasite Trypanosoma cruzi 55 aneuploidies 55 invasive lobular 55 Chronic Kidney 55 hypertrophic cardiomyopathy HCM 55 congenital hypothyroidism 55 Diamond Blackfan Anemia 55 Sclerosing 55 CHDs 55 cholangiocarcinoma 55 mycobacterium tuberculosis 55 brucella 55 prematurity ROP 55 GRNOPC1 contains 55 myelodysplasia 55 progressive neurodegenerative disease 55 parvovirus B# 55 T1DM 55 reactive airway 55 genital human papillomavirus 55 bacteria Pseudomonas aeruginosa 55 interstitial nephritis 55 non mutated KRAS 55 H. influenzae 55 Lower Genital Tract 55 unknown etiology 55 Newborn screening 55 Urinary tract infection 55 Duchenne Becker 55 amebiasis 55 Chlamydia pneumoniae 55 torsade de pointes 55 inflammatory rheumatic 55 Herpes Simplex 55 Equine piroplasmosis 55 karyotypes 55 Angelman 55 mutated BRCA 55 somatic mutation 55 urogenital infections 55 neovascularisation 55 Prevotella 55 pathophysiologic 55 MDR Gram negative 55 polycystic ovarian disease 55 Histoplasma capsulatum 55 chronic eosinophilic leukemia 55 PTPN# 55 aeruginosa 55 Associated Adipose Redistribution 55 Vulvar 55 degenerative neurological condition 55 Vaccine Shows Promise 55 Antisocial personality 55 Wilm tumor 55 noncontagious 55 Subtype 55 Chronic fatigue 55 familial ALS 55 HLA DQ2 55 GH deficiency 55 severe dehydrating diarrhea 55 bullous 55 rheumatological 55 Ankylosing spondylitis 55 S. suis 55 Churg Strauss syndrome 55 leukoencephalopathy 55 Chronic pancreatitis 55 Beta Thalassemia 55 Heavy menstrual bleeding 55 Creutzfeldt Jakob 55 Typhoid fever 55 BH4 deficiency 55 inflammatory bowel 55 TP# mutation 55 diabetes insipidus 55 Corynebacterium 55 brucei 55 microscopic colitis 55 bacterium Streptococcus 55 asthma rheumatoid arthritis 55 LCMV infection 55 Hypertriglyceridemia 55 Schizoaffective disorder 55 Rh factor 55 Atopic eczema 55 commercializes innovative biopharmaceuticals 55 allelic variants 55 Fabry Disease 55 fibrotic lung 55 Genital herpes 55 fibroma 55 PCNSL 55 Heartworm disease 55 tuberculous 55 Cognitive dysfunction 55 cervicitis 55 CTEPH 55 monogenic disorders 55 Leydig cell 55 Raynaud syndrome 55 immuno compromised individuals 55 hyperinsulinism 55 thyroid dysfunction 55 reproductive endocrine 55 Papillary 55 Neurodegenerative diseases 55 Frontotemporal Dementia 55 Polycystic Ovary Syndrome 55 Staphyloccus aureus 55 PLX STROKE targeting 55 orchitis 55 myeloproliferative diseases 55 neurosensory 55 androgenetic alopecia 55 Krabbe Leukodystrophy