Related by context. All words. (Click for frequent words.) 74 autosomal recessive disease 72 dominantly inherited 69 inherited neurodegenerative 68 spinal muscular atrophy SMA 68 Hereditary angioedema 68 dyskeratosis congenita 68 autosomal recessive genetic 68 chronic granulomatous disease 68 de novo mutations 68 Myocarditis 68 holoprosencephaly 67 Severe Combined Immunodeficiency 67 medium chain acyl 67 Ph + acute lymphoblastic 67 muscular dystrophy cystic fibrosis 67 cause cardiac channelopathies 67 neurodevelopment disorder 67 debilitating neurodegenerative disorder 67 Genetic mutation 67 Polycystic kidney disease 67 Tuberous sclerosis 67 Becker muscular dystrophy 67 Myotonic dystrophy 67 Arrhythmogenic Right Ventricular Cardiomyopathy 66 enterocolitis 66 Von Willebrand disease 66 progressive neurodegenerative disorder 66 progressive neurodegenerative 66 Meckel Gruber 66 Kufs disease 66 Fanconi anemia FA 66 Osteogenesis imperfecta 66 monogenic 66 nonhereditary 66 inflammatory demyelinating 66 Hutchinson Gilford progeria 66 Celiac sprue 66 multisystem disease 66 autosomal recessive disorder 66 Cystic fibrosis CF 66 neuropsychiatric disorder 65 Ribavirin causes 65 autosomal dominant disorder 65 recessive genetic 65 autosomal dominant polycystic kidney 65 degenerative disorder 65 Hurler syndrome 65 systemic amyloidosis 65 Ischemic heart 65 Crouzon Syndrome 65 sporadic Creutzfeldt Jakob 65 primary ciliary dyskinesia 65 neurodegenerative disorder characterized 65 von Hippel Lindau 65 Li Fraumeni syndrome 65 neurodegenerative disorder 65 neuro degenerative disease 65 progressive neuromuscular 65 Beta thalassemia 65 Ewing sarcoma bone 65 gastrointestinal dysfunction 65 Krabbe Leukodystrophy 65 immuno deficiency 65 Medulloblastoma 65 alpha1 antitrypsin deficiency 65 Hypertrophic cardiomyopathy 65 Acute myeloid leukemia 65 multisystem disorder 64 cystic fibrosis muscular dystrophy 64 Lafora disease 64 chronic autoimmune disorder 64 leptin deficiency 64 Congenital Adrenal Hyperplasia 64 fatal neurodegenerative 64 Alport Syndrome 64 fatal neurodegenerative disorder 64 bacterium Mycobacterium tuberculosis 64 nephrosis 64 transfusion syndrome 64 Magnesium deficiency 64 metachromatic leukodystrophy 64 Canavan Disease 64 neuro degenerative 64 embryonal rhabdomyosarcoma 64 Retinitis pigmentosa 64 Variant Creutzfeldt Jakob Disease 64 neuro developmental disorder 64 Hypophosphatasia 64 Genetic predisposition 64 Sporadic CJD 64 Spinal Muscular Atrophy SMA 64 Hurler Syndrome 64 deafness neurological 64 Glioblastoma multiforme GBM 64 retinal dysfunction 64 hereditary spastic paraplegia 64 enteroviral infection 64 rare chromosomal disorder 64 immunodeficiencies 64 Chronic lymphocytic leukemia 64 cystic fibrosis Duchenne muscular 64 tuberous sclerosis complex 64 NPHP 64 Cockayne syndrome 64 Hypertensive heart 64 Childhood Disorder 64 Pulmonary fibrosis 64 aneuploidies 64 chromosomal anomaly 63 medulloblastoma tumors 63 degenerative neurological disease 63 Neural tube defects 63 Nonalcoholic fatty liver 63 Fanconi Anemia 63 severe congenital neutropenia 63 Endometrial cancer 63 myopathies 63 Polycystic ovary syndrome PCOS 63 immunodeficiency disorder 63 autoinflammatory diseases 63 ADPKD 63 galactosemia 63 Von Hippel Lindau 63 Myasthenia gravis 63 progressive degenerative neurological 63 mitochondrial disorders 63 spastic diplegia 63 cystic fibrosis sickle cell 63 severe malignant osteopetrosis 63 Myocardial infarction 63 Pulmonary hypertension 63 Systemic lupus erythematosus 63 G6PD deficiency 63 ectodermal dysplasia 63 TTR amyloidosis 63 Alagille syndrome 63 Tay Sachs thalassemia 63 Pneumococcal pneumonia 63 recessively inherited 63 autosomal recessive 63 chromosomal disorder 63 congenital muscular dystrophy 63 Fatty liver 63 neuro developmental disorders 63 incurable neurological disorder 63 Cerebral malaria 63 pancreatic endocrine 63 pneumonia septicemia 63 Histiocytosis 63 Rh incompatibility 63 inherited neurological disorder 63 ANCA associated 63 Autoimmune hepatitis 63 Cryptococcus neoformans 63 oligodendrogliomas 63 chromosome abnormality 63 Atopic dermatitis 63 fronto temporal dementia 63 Cholangiocarcinoma 63 Brugada Syndrome 63 Neurofibromatosis type 63 neonatal lupus 63 hypereosinophilic syndrome 63 hereditary deafness 63 congenital disorders 63 kidney urologic 63 Oxidative damage 63 Leukemias 63 systemic mastocytosis 63 Folic acid deficiency 62 Apert syndrome 62 progressive neurodegenerative disorders 62 craniofacial abnormalities 62 Henoch purpura 62 bone marrow mesenchymal stem 62 progressive retinal degenerative 62 fatal myelination disorder 62 Sandhoff disease 62 smoldering myeloma 62 Alport syndrome 62 genetic syndromes 62 opsoclonus myoclonus syndrome 62 myelogenous leukemia 62 CHARGE syndrome 62 familial dysautonomia 62 SSc 62 cystic fibrosis chronic pancreatitis 62 Hirschsprung disease 62 chronic myeloid 62 Sanfilippo Syndrome 62 Invasive pneumococcal disease 62 spinocerebellar ataxia type 62 seizures comas 62 chromosomal defect 62 genetic lysosomal storage 62 Uncontrolled hypertension 62 hepatocellular carcinoma liver 62 phenotypic expression 62 Angelman syndrome 62 muscular dystrophy cerebral palsy 62 bronchopulmonary dysplasia BPD 62 Chronic pancreatitis 62 retinitis pigmentosa degenerative 62 Chronic lymphocytic leukemia CLL 62 hemophagocytic lymphohistiocytosis 62 childhood disintegrative disorder 62 Krabbe Disease 62 Aortic stenosis 62 congenital deafness 62 mosaicism 62 Muscular dystrophy 62 mental retardation blindness 62 Viral infections 62 inappropriate antidiuretic hormone SIADH 62 Down syndrome spina bifida 62 mitochondrial myopathy 62 neurological disorder affecting 62 esthesioneuroblastoma rare form 62 AAT deficiency 62 glutamic acid decarboxylase 62 coma convulsions 62 Zinc deficiency 62 Niemann Pick disease 62 Bronchopulmonary Dysplasia 62 BMPR2 62 #q# deletion 62 Adrenoleukodystrophy 62 Severe Primary IGFD 62 Diamond Blackfan anemia 62 maternally transmitted 62 Ischaemic heart 62 paraneoplastic 62 ceroid lipofuscinosis NCL 62 Spina bifida 62 Respiratory syncytial virus 62 monozygotic twin 62 pulmonary hypoplasia 62 MELAS 62 channelopathies 61 inherited neurodegenerative disorder 61 Creutzfeld Jakob disease 61 WAGR syndrome 61 undiagnosed celiac disease 61 XMRV retrovirus 61 lichen planus 61 C1 INH deficiency 61 Basal Cell 61 Systemic lupus erythematosus SLE 61 hypokalemia hypomagnesemia 61 leukodystrophies 61 hereditary predisposition 61 CMV infections 61 incurable neurodegenerative disease 61 neuro degenerative disorder 61 Hutchinson Gilford Progeria Syndrome 61 discoid lupus 61 sickle cell cystic fibrosis 61 Genetic variations 61 velo cardio facial 61 recessive dystrophic epidermolysis bullosa 61 Genetic variants 61 achromatopsia 61 Autoimmune disorders 61 Wiskott Aldrich Syndrome 61 Hereditary angioedema HAE 61 Aplastic anemia 61 multi infarct dementia 61 Lou Gehrigs disease 61 systemic autoimmune 61 Streptococcus agalactiae 61 Tay Sachs Disease 61 chronic obstructive airway 61 Diabetic nephropathy 61 polycystic kidneys 61 bronchopulmonary dysplasia 61 chronic eosinophilic leukemia 61 meningitis encephalitis 61 CHD7 61 Genetic mutations 61 mastocytosis 61 hemorrhagic colitis 61 cardiac channelopathies 61 Maternal obesity 61 spinal muscle atrophy 61 Motor neurone disease 61 GPC5 61 SOD2 gene 61 Huntingtons disease 61 Diabetic neuropathy 61 fat malabsorption 61 Phenylketonuria PKU 61 retinal degenerative disease 61 Eisenmenger syndrome 61 infertility miscarriages 61 renal failure interstitial lung 61 predisposing factor 61 mental retardation epilepsy 61 treat musculoskeletal metabolic 61 Papillary 61 Hemiplegia 61 histiocytosis 61 Porphyria 61 muscle degeneration 61 nerve degeneration 61 Joubert syndrome 61 homocystinuria 61 myeloproliferative 61 Noonan Syndrome 61 ADA SCID 61 fatal neuromuscular disorder 61 spina bifida cerebral palsy 61 metabolic abnormality 61 mutated K ras 61 MYH9 gene 61 collagen vascular 61 inherited retinal degeneration 61 severe dehydrating diarrhea 61 aMCI precursor 61 Iron deficiency anemia 61 histologically active 61 eczema hay fever 61 refractory Hodgkin 61 Anencephaly 61 neurogenetic 61 #q#.# deletion syndrome 61 progressive degenerative 61 pseudotumor cerebri 61 hereditary disorders 61 lateral sclerosis ALS 61 myelomeningocele 61 vitamin B1 deficiency 61 hyper IgE syndrome 61 Valvular heart 61 recessive trait 61 Biliary atresia 61 Epstein Barr Virus 61 Relapsing remitting MS 61 skeletal dysplasia 61 enteroviral 61 psychosis schizophrenia 61 polymorphic ventricular tachycardia 61 Rhesus disease 61 Pompe Disease 61 hereditary degenerative 61 thalassemia sickle cell 61 Pleural mesothelioma 61 osteogenesis imperfecta OI 61 Pelizaeus Merzbacher disease 61 epilepsy cerebral palsy 61 cystic kidney 61 bacteria Neisseria meningitidis 61 clinically heterogeneous 61 gene MECP2 61 Duchene muscular dystrophy 61 leukodystrophy 61 disorder Creutzfeldt Jakob 61 HLA DR4 61 Polycystic ovarian syndrome 61 encephalitis swelling 60 chronic lymphocytic 60 Pelvic inflammatory 60 membranous nephritis 60 Acute Myelogenous Leukemia 60 Eclampsia 60 enteropathy 60 progressive neurodegenerative disease 60 neurodevelopmental disorder 60 limb malformations 60 incurable genetic 60 Pervasive Developmental Disorders 60 plaque buildup restricts 60 variable immunodeficiency 60 hereditary disorder 60 diffuse intrinsic pontine glioma 60 Sudden infant 60 hyperinsulinism 60 incurable degenerative 60 Dilated cardiomyopathy 60 hemoglobinopathies 60 inherited genetic mutations 60 histologic subtype 60 idiopathic pulmonary 60 SMN1 60 Dental caries 60 Diffuse Intrinsic Pontine Glioma 60 Folate deficiency 60 hip osteonecrosis avascular 60 developmental abnormalities 60 erythema nodosum 60 filaggrin 60 nephronophthisis 60 Morquio Syndrome 60 Metastases 60 Usher Syndrome 60 trophoblastic 60 xeroderma pigmentosum 60 Coeliac disease 60 autosomal dominant 60 Interstitial cystitis 60 VCFS 60 induced cardiomyopathy 60 Dravet syndrome 60 Ehlers Danlos syndrome 60 Diabetic Ketoacidosis 60 diabetic kidney 60 tryptase 60 1 diabetes T1D 60 Epstein Barr Virus EBV 60 Variant CJD 60 Krabbe leukodystrophy 60 potent inducer 60 cytomegalovirus infection 60 microdeletion 60 inherited retinal 60 included exfoliative dermatitis 60 Hemolytic uremic syndrome 60 abnormal p# 60 hyperparathyroidism 60 superior mesenteric artery 60 Leber Congenital Amaurosis LCA 60 GRNOPC1 contains 60 hemolytic disease 60 orchitis 60 Dystrophin 60 acute myeloid 60 blastoma 60 genetically inherited 60 Treacher Collins 60 autoimmune encephalitis 60 malarial anemia 60 valvular heart disease 60 IgA deficiency 60 lysosomal storage disease 60 Newborn screening 60 Epstein Barr virus EBV 60 Histoplasmosis 60 disorder thalassemia 60 neuro degenerative disorders 60 hypertrophic cardiomyopathy HCM 60 nongenetic 60 neurodevelopmental disorder characterized 60 Polycythemia vera 60 Amyotrophic lateral sclerosis ALS 60 neurobehavioral disorder 60 Genital herpes 60 curing muscular dystrophy 60 multiple sclerosis lupus 60 motor neuron degeneration 60 1 Antitrypsin Deficiency 60 osteopetrosis 60 causative genes 60 Benign tumors 60 Proteus syndrome 60 invasive fungal 60 MCAD deficiency 60 SNT-MC#/idebenone 60 Hemorrhagic 60 epidermolysis bullosa EB 60 Jakob Disease 60 BRAF V#E 60 congenital toxoplasmosis 60 testicular tumors 60 Malignant glioma 60 familial clustering 60 Lesch Nyhan syndrome 60 myotonic dystrophy 60 underlying pathophysiology 60 arterial calcification 60 Parkinson disease multiple sclerosis 60 Polymorphic Ventricular Tachycardia CPVT 60 inherited mutations 60 pathological hallmark 60 erythematosus 60 bacterium Neisseria meningitidis 60 Bardet Biedl syndrome 60 Familial hypercholesterolemia 60 subependymal giant cell 60 prematurity ROP 60 Congenital heart 60 alveolar rhabdomyosarcoma 60 Chronic Lung 60 incurable degenerative brain 60 Dwarfism 60 Opportunistic infections 60 roseola 60 autoimmune thyroid 60 spongiform encephalopathies 60 nonbacterial prostatitis 60 rheumatoid arthritis lupus 60 exocrine glands 60 chromosomal disorders 60 acute lymphoblastic 60 leukemia lymphomas 60 Ewings sarcoma 60 aciduria 60 Associated Adipose Redistribution 60 Pulmonary arterial hypertension 60 neuroblastoma tumor 60 Congenital Muscular Dystrophy 60 Mitochondrial diseases 60 Gestational diabetes 60 Leber congenital amaurosis 60 progranulin gene 60 idiopathic pulmonary arterial hypertension 60 non polyposis colorectal 60 muscular dystrophy multiple sclerosis 60 Duchenne muscular dystrophy DMD 60 motor neurones 60 deCODE BreastCancer 60 multisystemic 60 Upregulation 60 pathological hallmarks 60 CRTAP 60 hay fever allergic rhinitis 60 prenatally diagnosed 59 juvenile myelomonocytic leukemia 59 idiopathic PAH 59 thrombophilia 59 chronic inflammations 59 Niemann Pick 59 thyroid hormone deficiency 59 PLX STROKE targeting 59 Human papillomavirus 59 hereditary nonpolyposis colorectal cancer 59 MEF2A 59 humans variant Creutzfeldt 59 chromosome #q#.# deletion 59 spontaneous mutation 59 debilitating neurological disease 59 chronic rheumatic 59 Ohtahara syndrome rare 59 lymphoproliferative disease 59 familial polyposis 59 neurodevelopmental disability 59 epidermolysis bullosa 59 paralysis blindness 59 JAK2 enzyme 59 Brugada syndrome 59 Idiopathic pulmonary fibrosis IPF 59 familial adenomatous polyposis FAP 59 osteogenesis imperfecta 59 Graft Versus Host 59 Thyroid hormone 59 Hp2 2 59 parasite Plasmodium falciparum 59 Vaccine Shows Promise 59 facioscapulohumeral muscular dystrophy 59 Prenatal diagnosis 59 congenital adrenal hyperplasia CAH 59 ADAMTS# 59 molecular abnormalities 59 disease Chronic Traumatic 59 Akt signaling 59 Hyperkalemia 59 Dysplasia 59 genes predisposing 59 Premature Aging 59 Anaplasmosis 59 Entamoeba histolytica 59 pulmonary thromboembolism 59 congenital deficiency 59 DiGeorge Syndrome 59 lactase deficiency 59 Lichen planus 59 cerebral vascular disease 59 Acne vulgaris 59 LRP5 59 allergic airway 59 insulin secreting beta 59 Stargardt Macular Dystrophy 59 HGPS 59 degenerative neurological disorder 59 Mitochondrial disease 59 Retinitis Pigmentosa RP 59 SMN protein 59 synovial cells 59 microchimerism 59 multiorgan 59 treating sarcoma testicular 59 gastric carcinoma 59 renal fibrosis 59 obstructive coronary artery 59 renovascular hypertension 59 CCR5 delta# 59 cystic fibrosis hereditary 59 HbF 59 pneumonia sepsis 59 Gliomas 59 chromosomal anomalies 59 maternally inherited 59 MECP2 gene 59 breast endometrial 59 nephropathy kidney 59 JAK mutations 59 Atopic eczema 59 PARP inhibition 59 Leber congenital amaurosis LCA 59 fibrotic lung 59 commonest cause 59 autoinflammatory 59 Langerhans cell histiocytosis 59 comorbid anxiety 59 persistent pulmonary hypertension 59 bacteria Mycobacterium tuberculosis 59 Myopathy 59 leukemias lymphomas 59 flaccid paralysis 59 necrotising enterocolitis 59 Von Willebrand 59 AAT Deficiency 59 Subarachnoid hemorrhage 59 tricuspid atresia 59 Sjogren Syndrome 59 cirrhosis liver failure 59 tumor subtype 59 blindness paralysis 59 Neisseria 59 muscular dystrophies 59 GH deficiency 59 Premature Ovarian Failure 59 neuro endocrine 59 Marfan Syndrome 59 multifactorial disease 59 Thorough cooking kills 59 extramedullary 59 Lewy Body 59 leukemia lymphoma multiple myeloma 59 Patau syndrome 59 degenerative nerve disorder 59 Crohns disease 59 debilitating neurodegenerative 59 thyroid deficiency 59 post transplant lymphoproliferative 59 ARVD 59 protein misfolding diseases 59 epigenetic changes 59 progeria rare 59 cutaneous lupus 59 cisplatin resistant 59 Neural tube 59 Ectopia Cordis 59 promyelocytic leukemia 59 meningitis encephalitis pulmonary edema 59 dysgenesis 59 myotonic muscular dystrophy 59 NQO1 59 autosomal dominant inheritance 59 multi factorial disease 59 Polycystic Kidney Disease 59 Radiographic findings 59 Oppositional Defiant Disorder 59 Salmonella typhi 59 hereditary pancreatitis 59 auditory neuropathy 59 Fanconi anemia 59 Wolf Hirschhorn 59 intraventricular hemorrhage 59 degenerative neuromuscular disease 59 spastic paraplegia 59 Hutchinson Gilford Progeria 59 encephalitis meningitis 59 Lymphocytic 59 teratogens 59 diseases chronic granulomatous 59 heterotaxy 59 syngeneic 59 monogenic disorders 59 amputation blindness 59 blood clotting disorder 59 hormonally sensitive 59 Wilm Tumor 59 arthritis lupus 59 Derek Besenfelder 59 MCADD 59 extrapulmonary disease 59 periodontal tissues 59 haemolytic uraemic syndrome 59 Trypanosoma brucei 59 Dysautonomia 59 herpesviruses 59 acute lymphoid leukemia 59 neuropsychiatric diseases 59 imperfecta 59 reproductive endocrine 59 Meckel Gruber syndrome 59 Arrhythmogenic 59 autoimmune uveitis 59 HLA DRB1 59 neuronal dysfunction 59 gastrointestinal stromal tumor 59 lupus multiple sclerosis 59 progressive degeneration 59 Peritoneal mesothelioma 59 Tay Sachs disease 59 Acute Respiratory Failure 59 CFTR gene 59 cardiomyopathy weakening 59 Wilm tumor 59 mycosis fungoides 59 Hashimoto thyroiditis 59 debilitating neurological disorder 59 Li Fraumeni 58 Pernicious anemia 58 cervix uteri 58 abnormal lymphocytes 58 thrombocytopenia neutropenia 58 ataxias 58 Hip dysplasia 58 lymphomas leukemias 58 Crouzon syndrome 58 prion protein PrP 58 Chiari malformation 58 Benign breast 58 Parathyroid 58 Myelodysplastic syndrome 58 lupus scleroderma 58 congential 58 triggers apoptosis programmed 58 Alzheimer disease vascular dementia 58 Holoprosencephaly 58 McCune Albright 58 neuritic 58 Cognitive dysfunction 58 dystrophies 58 unexplained mental retardation 58 Androgenetic alopecia 58 urologic diseases 58 Acute lymphoblastic leukemia 58 DiGeorge syndrome 58 gastrointestinal stromal tumors GISTs 58 Lipodystrophy 58 Cytotoxic T 58 Smith Lemli Opitz syndrome 58 wasting Creutzfeldt Jakob 58 autoimmune disorders asthma 58 Glioblastoma Multiforme GBM 58 Fragile X gene 58 DIPG 58 dermatologic reactions 58 cardiovascular endocrine 58 hematologic disorders 58 lysosomal storage disorder 58 Study Spacing 58 septicemic 58 neuropathic pain spasticity 58 cortical dysplasia 58 Essential tremor 58 Cerebral palsy involves 58 meningitis sepsis 58 Williams Beuren syndrome 58 Wilms Tumor 58 Rotavirus causes 58 Infant botulism 58 neurological sequelae 58 neurocognitive dysfunction 58 myeloproliferative neoplasms 58 fetal malformations 58 Balamuthia 58 Chronic myeloid leukemia CML 58 hypophosphatasia 58 Clusterin 58 CDH1 58 Parkinson disease neurodegenerative disorder 58 PCA3 gene 58 coagulopathy 58 kidney fibrosis 58 obesity insulin resistance 58 pancreas esophagus 58 damage cirrhosis liver 58 melanocortin receptor 58 asthma emphysema bronchitis 58 Tuberous Sclerosis 58 molar pregnancy 58 neurofibrillary 58 apolipoprotein E4 58 LRAT 58 hereditary hemochromatosis 58 R#W [002] 58 renal kidney 58 BRAF gene mutations 58 degenerative neurological condition 58 Cancer cachexia 58 spontaneous miscarriages 58 vesicular stomatitis virus 58 Rubinstein Taybi syndrome 58 carbohydrate intolerance 58 gestational diabetes mellitus GDM 58 bacterium Streptococcus 58 hyperphenylalaninemia HPA due 58 familial aggregation 58 hormonal abnormalities 58 mitochondrial mutations 58 infertility miscarriage 58 Squamous Cell 58 Retinopathy 58 advanced glycation endproducts 58 herpes encephalitis 58 dilated cardiomyopathy DCM 58 differential gene expression 58 BCR ABL protein 58 Fragile X Syndrome 58 Chronic fatigue 58 deafness meningitis 58 KIBRA 58 Pancreatic insufficiency 58 Combined Immune Deficiency 58 NPM1 gene 58 pulmonary metastasis 58 progressively degenerative 58 Cojocaru correspondent 58 biliary atresia rare 58 familial pancreatic cancer 58 Maroteaux Lamy syndrome 58 Meningiomas 58 Crigler Najjar syndrome 58 Factor XIII 58 Anorexia nervosa 58 proband 58 Glucocorticoid 58 urinary bladder wall 58 plexiform 58 degenerative motor neuron 58 acute porphyria 58 congenita 58 Vascular dementia 58 Amyotrophic lateral sclerosis 58 Wiskott Aldrich syndrome 58 nonbacterial 58 Menopausal hormone therapy 58 renal scarring 58 hormonal disorder 58 Treatment Shows Promise 58 neuronal ceroid lipofuscinosis 58 fatal neuromuscular 58 insulin secreting islet cells 58 Ivanhoe Newswire Patients 58 liver decompensation 58 thoracic aortic aneurysm 58 anemias 58 chronic progressive neurodegenerative 58 leukoencephalopathy 58 mucus glands 58 etiologic agent 58 Fibroblast 58 contagious bacterial infection 58 MELAS syndrome 58 susceptibility alleles 58 seizures miscarriages 58 HHV 6 58 T1DM 58 Hypertrophy 58 Uncontrolled diabetes 58 ependymoma 58 bacteremic pneumonia 58 underactive thyroid gland 58 Genetic variation 58 Peutz Jeghers syndrome 58 Hyperthyroidism 58 Lupus nephritis 58 chronic degenerative 58 Nephrogenic Systemic Fibrosis NSF 58 Inhaled nitric oxide 58 cerebri 58 Retinoblastoma 58 brain malformation 58 Menkes disease 58 Philadelphia Chromosome Positive 58 aphthous stomatitis 58 epilepsy Parkinson disease 58 complement inhibitor eculizumab 58 neonatal encephalopathy 58 1 proteinase inhibitor 58 congenital hypothyroidism 58 gynecologic malignancy 58 hepatorenal syndrome 58 Heavy snorers 58 complex neurobiological disorder 58 HLA identical 58 Ectodermal Dysplasia 58 Fanconi anemia rare 58 choriocarcinoma 58 inhibitory receptor 58 fibrosarcoma 58 ERK signaling 58 leukemia multiple myeloma 58 Down syndrome chromosomal disorder 58 polydactylism 58 psychosocial dwarfism 58 endocrine disorder 58 developing Surfactant Therapies 58 congenital diaphragmatic hernia 58 mutated BRCA 58 heritable diseases 58 asthma rheumatoid arthritis 58 K ras mutations 58 Epidermolysis bullosa 58 adrenal hormones 58 rheumatoid arthritis inflammatory bowel 58 type 1diabetes 58 hypertension cardiovascular disease 58 Selenium deficiency 58 atypical parkinsonism 58 Squamous cell 58 IRAK1 58 arteritis 58 antiphospholipid antibodies 58 herpes zoster virus 58 Neisseria meningitidis bacteria 58 1 antitrypsin AAT 58 autism dyslexia 58 Bordetella pertussis 58 Asperger syndrome milder 58 unprovoked seizures 58 Polyneuropathy 58 neurological dysfunction 58 lymphoma myeloma 58 neurobiological disorder 58 Guillain Barré Syndrome 58 Reye syndrome rare 58 endocrine dysfunction 58 aplastic 58 prostate carcinogenesis 58 Vitamin B# deficiency 58 sickle cell hemoglobin 58 HELLP 58 fibroma 58 hypothalamic pituitary adrenal axis 58 Glioma 58 nephritis 58 NECK CANCER SUPPORT GROUP 58 6 phosphate dehydrogenase 58 mGluR4 activation 58 ABCB1 58 rare autosomal recessive 58 Foetal 58 amyloid cascade 58 attach auristatin 58 alpha thalassemia 58 de ath 58 human leukocyte antigen HLA 58 Prion diseases 58 Phenylketonuria 58 SIADH 58 causative mutation 58 Hemolytic Uremic Syndrome 58 Papillomavirus 58 2 diabetes T2D 58 Neurofibromatosis 58 IPAH 58 Hemochromatosis 58 Hypertrophic 58 SMN1 gene 58 human leukocyte antigens 58 Arnold Chiari Malformation 58 Rhabdomyosarcoma 58 polyhydramnios 58 degenerative neurological diseases 58 levodopa induced 58 amputations blindness 58 Therapies SRT 57 PCNSL 57 Stress urinary incontinence 57 multiple sclerosis amyotrophic lateral 57 congenital CMV 57 deletion 5q 57 stem glioma 57 Tourette Syndrome TS 57 chromosome #q#.# [001] 57 dystrophy 57 CFTR gene mutations 57 Glomerular 57 Arteriosclerosis 57 genetic loci 57 generalized epilepsy 57 cardiovascular restenosis cancer 57 insulin resistance syndrome 57 murine leukemia virus 57 encephalitis inflammation 57 neurologic deficits 57 genetic abnormality 57 Acute lymphocytic leukemia 57 BRCA1 BRCA2 57 multivessel coronary artery 57 Idiopathic pulmonary fibrosis 57 Sclerosing 57 granulosa cell 57 polycystic 57 Alopecia Areata 57 monozygotic twins 57 brain lesions 57 familial ALS 57 pancreatic islet 57 Predisposition 57 Chronic ITP 57 oral thrush 57 regulator CFTR gene 57 destroys myelin 57 Gene Mutation Linked 57 inherited metabolic disorders