Related by context. All words. (Click for frequent words.) 77 onset Alzheimer 64 Alzheimer disease 62 dementia 59 Alzheimer disease AD 58 FTLD 57 LQTS 57 Alzheimers disease 57 neurodegenerative disorder 57 APOE gene 57 incurable neurological disorder 56 degenerative disorder 55 Alzheimer 55 neurodegenerative disease 55 frontotemporal dementia 55 progressive neurological disorder 54 Angelman syndrome 54 Parkinson disease 54 progressive neurodegenerative disorder 54 degenerative brain 53 cognitive impairment 53 familial adenomatous polyposis 53 ovarian cancer 53 HER2 positive breast cancer 53 myotonic dystrophy 53 Fanconi anemia 53 Alzheimer Disease 53 fatal neuromuscular disorder 53 degenerative neurological disorder 53 genetic abnormalities 53 ApoE4 gene 52 hereditary breast cancer 52 lung cancer 52 Testicular cancer 52 vascular dementia 52 KIBRA 52 fungal meningitis 52 sporadic ALS 52 familial pancreatic cancer 52 Parkinson disease neurological disorder 52 genetic mutations 52 alzheimer disease 52 colorectal cancer 52 familial ALS 52 onset sepsis 52 Fragile X 52 progressive neurodegenerative disease 51 NF1 51 Polycystic kidney disease 51 genetic disorders 51 hereditary nonpolyposis colorectal cancer 51 mild cognitive impairment 51 invasive breast cancer 51 APOE 51 chromosome abnormality 51 APOE ε4 51 Muscular dystrophy 51 Tay Sachs disease 51 motor neuron disease 51 Lewy Body Dementia 51 genetic abnormality 51 autism spectrum disorders 51 frontal lobe dementia 51 Dravet syndrome 51 systemic scleroderma 51 degenerative neurological disease 51 breast cancer 51 Parkinson disease PD 50 inherited neurological disorder 50 gene variation 50 APOE4 50 Alzheimers Disease 50 gene APOE4 50 Kufs disease 50 schizophrenia 50 spinocerebellar ataxia 50 hereditary disorder 50 Obstructive sleep apnea 50 HNPCC 50 frontal temporal dementia 50 SORL1 50 GBA mutations 50 colon cancer 50 Parkinson Disease 50 dementias 50 holoprosencephaly 50 Alzheimer Disease AD 50 FXTAS 50 ADPKD 50 fatal neurodegenerative disorder 50 endometrial cancer 50 Parkinsons disease 50 neuro degenerative disorder 50 fronto temporal dementia 50 Rett syndrome 50 Major depressive disorder 50 acute myelogenous leukemia AML 50 G#S mutation 49 prediabetes 49 inherited mutations 49 malignant mesothelioma 49 AAT deficiency 49 gene variant 49 MCAD deficiency 49 narcolepsy cataplexy 49 onset diabetes 49 bile duct cancer 49 apolipoprotein E APOE 49 genetic variations 49 Usher Syndrome 49 juvenile myelomonocytic leukemia 49 rheumatic disease 49 Cystic fibrosis 49 bowel cancer 49 acute myeloid leukemia 49 cognitive decline 49 colorectal cancers 49 inherited neurodegenerative disorder 49 chromosomal defect 49 prostate cancer 49 mitochondrial diseases 49 psychotic illness 49 Polycystic ovary syndrome PCOS 49 Cystic fibrosis CF 49 chromosomal disorder 49 Huntington Disease 49 APOE allele 49 Peanut allergies 49 progressive neurodegenerative 49 sarcopenia 49 Alzheimer pathology 49 Pompe Disease 49 genetic disorder 49 Motor neurone disease 49 Stomach cancer 49 mutated BRCA1 49 Postnatal depression 49 chromosomal abnormalities 49 Krabbe Disease 49 autism spectrum disorders ASDs 49 Brugada Syndrome 49 Amyotrophic lateral sclerosis ALS 49 Marfan syndrome 49 preterm deliveries 49 Schizophrenia 49 myelogenous leukemia 49 Cardiomyopathy 49 neurological disorder 48 incurable autoimmune 48 irreversible blindness 48 onset puberty 48 gene mutations 48 blight fungal 48 carcinoid cancer 48 genetic mutation 48 incurable lung cancer 48 endometrial cancers 48 fatal neurodegenerative 48 NAFLD 48 Dementia 48 Li Fraumeni syndrome 48 Cholangiocarcinoma 48 mitochondrial dysfunction 48 Leber Congenital Amaurosis LCA 48 cognitively normal 48 pancreatic cancer 48 Joubert Syndrome 48 immunodeficiency disease 48 kidney disease 48 Joubert syndrome 48 neuropsychiatric disorder 48 postoperative delirium 48 Meckel Gruber 48 gene mutation 48 progressive degenerative 48 heart disease 48 liver disease 48 Alport Syndrome 48 interstitial pulmonary fibrosis 48 polycystic ovary syndrome PCOS 48 Uterine cancer 48 preeclampsia 48 oesophageal cancer 48 ARVD 48 autism spectrum disorder 48 genetic syndromes 48 Fragile X syndrome 48 ventricular dysplasia 48 APOE e4 48 Peanut allergy 48 lupus 48 debilitating migraine headaches 48 incurable genetic 48 familial hypercholesterolemia 48 spinal muscle atrophy 48 LRRK2 mutations 48 Lewy Body 48 cardiomyopathy 48 psychotic illnesses 48 Huntington Chorea 48 primary progressive aphasia 48 Amyotrophic lateral sclerosis 48 myeloproliferative neoplasms 48 Guillain Barré Syndrome 48 disease NAFLD 48 spastic paraplegia 48 myalgic encephalomyelitis ME 48 Lou Gherig disease 48 frontotemporal dementia FTD 48 Lou Gerhig disease 48 Spinal Muscular Atrophy 48 Lewy Body dementia 47 Alzheimers 47 VCFS 47 Angelman Syndrome 47 AAT Deficiency 47 disabling neurological 47 intractable epilepsy 47 mitochondrial myopathy 47 Polycystic Kidney Disease 47 amyotrophic lateral sclerosis 47 colorectal polyps 47 tardive dyskinesia 47 Lewy body 47 CALHM1 47 degenerative disease 47 bronchopulmonary dysplasia 47 ApoE gene 47 Hashimoto thyroiditis 47 APOE e4 gene 47 BRCA1 mutations 47 subclinical hyperthyroidism 47 ectodermal dysplasia 47 degenerative neuromuscular disease 47 SRBD 47 Lou Gherig Disease 47 BRCA mutation 47 respiratory viral infections 47 disease 47 Parkinson disease neurodegenerative disorder 47 coronary disease 47 polycystic ovary syndrome 47 BRCA mutations 47 mutated gene 47 acute leukemias 47 Prematurity 47 autism 47 SORL1 gene 47 Fragile X Syndrome 47 hereditary predisposition 47 breast cancers 47 Down syndrome 47 amyotrophic lateral sclerosis ALS 47 Parkinson disease degenerative 47 invasive Hib 47 shorter telomeres 47 cystic fibrosis 47 Celiac disease 47 genetic variant 47 coronary artery disease 47 WNV infection 47 neuro degenerative disease 47 genetic defects 47 herpes simplex encephalitis 47 Pulmonary fibrosis 47 pneumococcal meningitis 47 HNSCC 47 myelodysplasia 47 TOMM# 47 genetic variants 47 bipolar disorder 47 ataxias 47 progressive supranuclear palsy 47 #q#.# [001] 47 sudden cardiac death 47 LRRK2 gene 47 Wiskott Aldrich Syndrome 47 inherited genetic mutations 47 Becker muscular dystrophy 47 Friedreich ataxia 47 polycystic disease 47 Crohn disease chronic 47 cardiovascular disease 47 diffuse gastric 47 genetic variants associated 47 preterm babies 47 Klinefelter syndrome 47 senile dementia 47 Postpartum depression 47 myeloid leukemia 47 Myasthenia gravis 47 chromosomal disorders 47 leukemia ALL 47 colon cancers 47 epidermolysis bullosa EB 47 sCJD 47 FMRP protein 47 dermatomyositis 47 Long QT Syndrome 47 cardiac channelopathies 47 pre eclampsia 47 Glioblastoma 47 Pulmonary hypertension 47 genetic variation 47 Alzheimer disease vascular dementia 47 celiac disease 47 elevated triglyceride levels 47 macular degeneration 46 Preeclampsia 46 monogenic diabetes 46 invasive secretory carcinoma 46 intestinal inflammation 46 Reye Syndrome 46 diagnosing Alzheimer disease 46 chronic lymphocytic leukemia CLL 46 Retinitis pigmentosa 46 incurable neurodegenerative disease 46 epilepsy 46 inherited retinal degeneration 46 cystinosis 46 related macular degeneration 46 compulsive hoarding 46 prion disease 46 Marfan Syndrome 46 olfactory dysfunction 46 uncontrolled epilepsy 46 Parkinson degenerative 46 neural tube defect 46 ovarian cancers 46 mutated genes 46 Mendelian diseases 46 rheumatoid arthritis 46 Von Willebrand disease 46 metabolic syndrome 46 Creutzfeldt Jakob 46 genes BRCA1 46 degenerative neurological condition 46 ataxia telangiectasia 46 chromosomal defects 46 Niemann Pick disease 46 PICALM 46 myasthenia gravis neuromuscular 46 menarche 46 medulloblastomas 46 FSGS 46 MYH9 gene 46 childhood leukemia 46 genetic defect 46 lymphangioleiomyomatosis LAM 46 penetrance 46 Aortic dissection 46 susceptibility gene 46 ASDs 46 Bipolar disorder 46 persistent pulmonary hypertension 46 rheumatoid arthritis RA 46 XMRV infection 46 lobular breast cancer 46 Multiple sclerosis MS 46 de ath 46 ATTR PN 46 Hemolytic Uremic Syndrome HUS 46 Krabbe disease 46 leukodystrophies 46 apolipoprotein E4 46 FMR1 gene 46 hypertrophic cardiomyopathy HCM 46 Cystic Fibrosis CF 46 blight pathogen 46 progressive multifocal leukoencephalopathy PML 46 biochemical imbalance 46 untreated sleep apnea 46 atypical hyperplasia 46 hemochromatosis 46 Leber congenital amaurosis LCA 46 Emphysema 46 de novo mutations 46 bladder cancer 46 cardiovascular disease CVD 46 DISC1 gene 46 ependymoma 46 metastatic cancer 46 MGUS 46 Parkinson Disease PD 46 Macular degeneration 46 mutant gene 46 systemic lupus erythematosus SLE 46 epigenetic changes 46 Barth Syndrome 46 aneuploidies 46 RSV infections 46 folate deficiency 46 leukemia 46 recurrent wheezing 46 medulloblastoma tumors 46 Takotsubo cardiomyopathy 46 systemic amyloidosis 46 Lewy bodies 46 chronic autoimmune disorder 46 Variant CJD 46 hyperemesis gravidarum 46 HELLP 46 BRCA2 gene 46 achondroplasia 46 CDH1 46 degenerative nerve disease 46 subclinical atherosclerosis 46 Von Hippel Lindau 46 dementing 46 liver cancer 46 Pericak Vance 46 Aortic stenosis 46 Lafora disease 46 generalized epilepsy 46 psychiatric disorders 46 basal cell nevus syndrome 46 Sanfilippo Syndrome 46 sporadic CJD 46 degenerative motor neuron 46 microvascular angina heart 45 HGPS 45 Premature birth 45 ApoE4 45 Chronic ITP 45 neurological disorder affecting 45 curable cancers 45 colorectal cancer CRC 45 glucose intolerance 45 menopause 45 vitamin D deficiency 45 neurofibromatosis type 45 dementing illness 45 homozygous familial hypercholesterolemia 45 Mild cognitive impairment 45 achromatopsia 45 T2D 45 genetically inherited 45 BRCA genes 45 neuromuscular disease 45 Tay Sachs 45 Hereditary angioedema HAE 45 ARVC 45 spinal muscular atrophy SMA 45 esophageal adenocarcinoma 45 cerebellar ataxia 45 Coeliac disease 45 medullary thyroid cancer 45 ruptured brain aneurysm 45 Li Huei Tsai 45 autism neurological disorder 45 Anorexia nervosa 45 TTR amyloidosis 45 Medulloblastoma 45 BRCA1 gene 45 Creutzfeldt Jakob disease 45 invasive pneumococcal disease 45 Cowden syndrome 45 multiple sclerosis 45 Aplastic anemia 45 CNTNAP2 45 macular disease 45 mitochondrial disease 45 susceptibility genes 45 squamous cell lung cancer 45 CHARGE syndrome 45 myelodysplastic syndrome MDS 45 Essential tremor 45 Friedrich Ataxia 45 systemic lupus erythematosus 45 Hutchinson Gilford progeria 45 Acute Myelogenous Leukemia 45 NOMID 45 Hip fractures 45 BRCA2 45 chromosome abnormalities 45 homozygous FH 45 degenerative nerve disorder 45 emphysema 45 debilitating autoimmune 45 amyloidosis 45 Hutchinson Gilford Progeria Syndrome 45 sclerosis ALS 45 Folate deficiency 45 perimenopause 45 benign proliferative breast 45 progranulin mutations 45 Alzheimer's 45 NF2 45 long QT syndrome 45 microalbuminuria 45 C. difficile infections 45 Generalized anxiety disorder 45 multiforme 45 coronary heart 45 testicular germ cell 45 pleural mesothelioma 45 Osteosarcoma 45 MCADD 45 Metabolic syndrome 45 incurable neurological 45 leukoencephalopathy PML 45 bone thinning 45 mitochondrial disorders 45 REM sleep behavior 45 Narcolepsy 45 perimenopausal women 45 depressive illness 45 Excessive daytime sleepiness 45 varicella zoster virus 45 neuroblastoma 45 T1DM 45 gene variants 45 primary ovarian insufficiency 45 disc degeneration 45 cognitive dysfunction 45 multiple sclerosis MS 45 symptomless 45 Colorectal cancers 45 COPD 45 precancerous cervical 45 FASPS 45 DQB1 * 45 cause cardiac channelopathies 45 CHD CVD 45 endometriosis 45 muscular dystrophy 45 Hurler syndrome 45 autosomal dominant polycystic kidney 45 lobular cancer 45 manic depressive disorder 45 Sudden Adult 45 preterm birth 45 alpha synuclein gene 45 1 diabetes T1D 45 Spinal Muscular Atrophy SMA 45 Brugada syndrome 45 Krabbe Leukodystrophy 45 autosomal dominant disorder 45 mood disorders 45 Fragile X. 45 Jill Stautner 45 Multiple sclerosis 45 developmental abnormalities 45 Chronic insomnia 45 chronic traumatic encephalopathy 45 Sjögren syndrome 45 muscular dystrophy cystic fibrosis 45 Maroteaux Lamy Syndrome 45 enterovirus infection 45 Genetic predisposition 45 cerebral infarction 45 Sporadic CJD 45 infectious syphilis 45 retinitis pigmentosa RP 45 paralytic polio 45 dopaminergic therapy 45 autosomal recessive 45 carotid atherosclerosis 44 neurodevelopmental disorders 44 CFTR gene 44 Gestational diabetes 44 cystic fibrosis hereditary 44 primary sclerosing cholangitis 44 COMT gene 44 Autism Spectrum Disorder 44 androgen deficiency 44 Chronic fatigue syndrome 44 neuro developmental disorder 44 esophageal cancers 44 TCF#L# gene 44 chronic lymphatic leukemia 44 defective gene 44 osteogenesis imperfecta 44 white matter hyperintensities 44 Krabbe leukodystrophy 44 Peutz Jeghers syndrome 44 neurological abnormalities 44 Creutzfeldt Jakob Disease 44 Beckwith Wiedemann syndrome 44 Ovarian cancer 44 prostate cancers 44 melanoma 44 benign breast 44 chronic lymphocytic leukemia 44 neurologic disorder 44 chlamydia infections 44 Vascular dementia 44 thoracic aortic disease 44 Non Hodgkin lymphoma 44 nonseminoma 44 low ptau levels 44 debilitating neurological disorder 44 Sickle cell 44 infection progressive multifocal 44 Duchenne muscular dystrophy 44 Diffuse Intrinsic Pontine Glioma 44 Dravet Syndrome 44 chlamydia infection 44 degenerative neurological diseases 44 postmenopause 44 Tay Sachs thalassemia 44 primary immunodeficiency 44 insulin resistance syndrome 44 Sarcopenia 44 IgA deficiency 44 neurobiological disorder 44 pemphigus 44 Duchenne Muscular Dystrophy DMD 44 Cryptococcus neoformans 44 Trisomy 44 Pompe disease 44 Endometrial cancer 44 diabetic nephropathy 44 autoimmune thyroiditis 44 nonsense mutations 44 Down syndrome chromosomal disorder 44 synovial sarcoma 44 mitochondrial mutations 44 disease Chronic Traumatic 44 febrile seizures 44 inherited genetic mutation 44 Autism Spectrum Disorders 44 premenstrual syndrome PMS 44 Overactive bladder 44 diabetic kidney 44 cancer 44 BRCA2 mutation 44 Physical inactivity 44 Migraines 44 subclinical hypothyroidism 44 hereditary hemochromatosis 44 aneuploidy 44 nonalcoholic fatty liver 44 Wilms tumor 44 retinitis pigmentosa 44 manic depressive illness 44 fatal neuromuscular 44 debilitating illness 44 Cirrhosis 44 acute myeloid leukemia AML 44 diabetes mellitus DM 44 dopamine receptor gene 44 breast cancer Narod 44 neurofibromatosis NF 44 inflammatory arthritis 44 alpha thalassemia 44 Bowel cancer 44 inflammatory bowel disease 44 Neurological disorders 44 proband 44 leukemia AML 44 acute promyelocytic leukemia 44 death syndrome SIDS 44 variable immunodeficiency 44 Noonan Syndrome 44 Long QT syndrome 44 cerebellar hypoplasia 44 V Leiden 44 autistic traits 44 BRCA gene mutation 44 nonmelanoma skin cancers 44 2 diabetes T2D 44 non hodgkins lymphoma 44 proliferative diabetic retinopathy 44 supranuclear palsy 44 myelin breakdown 44 eosinophilic esophagitis 44 cirrhosis liver failure 44 adenoid cystic carcinoma 44 inherited neurodegenerative 44 bronchopulmonary dysplasia BPD 44 neurodegenerative disorder characterized 44 heterozygous FH 44 parkinsonism 44 esophageal spams 44 neurobehavioral disorder 44 Pulmonary arterial hypertension 44 Depressive disorders 44 mild cognitive 44 chronic kidney 44 fibrodysplasia ossificans progressiva FOP 44 Genetic variants 44 diagnosed 44 APOE4 gene 44 juvenile idiopathic arthritis 44 Stargardt disease 44 progeria rare 44 Hypertrophic Cardiomyopathy 44 non syndromic 44 debilitating neurodegenerative 44 Anencephaly 44 atherosclerosis 44 esophageal cancer 44 hypertrophic cardiomyopathy 44 debilitating neurodegenerative disorder 44 Male pattern baldness 44 Prostate cancer 44 multiple myeloma 44 Progeria 44 microdeletions 44 prosopagnosia 44 pseudotumor cerebri 44 hemolytic anemia 44 allergic asthma 44 puerperal psychosis 44 ataxia 44 juvenile idiopathic arthritis JIA 44 dominantly inherited 44 Cockayne Syndrome 44 Genital herpes 44 malignant lymphoma 44 Epstein Barr virus 44 Haptoglobin 44 diabetes 44 multi infarct dementia 44 metachromatic leukodystrophy 44 autosomal dominant 44 invasive meningococcal disease 44 chronic granulomatous disease 44 muscular dystrophies 44 mutation 44 postmenopausal breast cancer 44 Apert syndrome 44 genetic susceptibility 44 FSHD 44 Parkinsons Disease 44 Autoimmune disorders 44 hereditary diseases 44 frontotemporal lobar degeneration 44 intellectual disability 44 neurodevelopmental disorder 44 Arrhythmogenic Right Ventricular Cardiomyopathy 44 liver fibrosis 44 myelodysplastic syndrome 44 #q# deletion syndrome 44 Rett Syndrome 44 Hypertrophic cardiomyopathy 44 leukoencephalopathy 44 Chronic angina 44 dyslexia 44 cystic fibrosis CF 44 WDR# 44 Nonalcoholic fatty liver 44 Tuberous Sclerosis 44 APOE genotype 44 Retinopathy 43 idiopathic pulmonary fibrosis IPF 43 arrhythmogenic right 43 Hutchinson Gilford Progeria 43 chronic neurological disorder 43 recessive genetic disorders 43 MYCN amplification 43 Alzheimer dementia 43 ductal breast cancer 43 primary IGFD 43 apolipoprotein E 43 vascular disease 43 relapsing remitting 43 neurological ailment 43 fatty liver disease 43 hypothyroidism 43 lymphoblastic lymphoma 43 dyscalculia 43 mild cognitive impairments 43 Hyperthyroidism 43 Hemochromatosis 43 chromosomal abnormality 43 hyperemesis 43 Sleep disordered breathing 43 chronic myeloid leukemia 43 type 1diabetes 43 neurodevelopmental 43 Mitochondrial diseases 43 nasopharyngeal carcinoma 43 monogenic 43 nasal pharyngeal cancer 43 Gastric cancer 43 gluten intolerance 43 Duchenne muscular dystrophy DMD 43 Joubert syndromes 43 polymorphic ventricular tachycardia 43 atypical ductal hyperplasia 43 TGFBR1 * 6A 43 Guillain Barré syndrome 43 atypical parkinsonism 43 causative gene 43 Malignant gliomas 43 reactive arthritis 43 ankylosing spondylitis 43 Glioblastoma Multiforme GBM 43 pneumococcal infection 43 brain shrinkage 43 malignant melanoma 43 Acute myeloid leukemia 43 gastrointestinal stromal tumor GIST 43 Pre eclampsia 43 BRCA gene 43 ε4 43 polycystic kidney disease 43 SHANK3 43 Hypophosphatasia 43 connective tissue disorder 43 fatal myelination disorder 43 aortic rupture 43 neuro muscular disease 43 Idiopathic pulmonary fibrosis 43 Rheumatoid arthritis 43 neurosyphilis 43 Rh incompatibility 43 Rotavirus infection 43 Retinoblastoma 43 Burkitt Lymphoma 43 dysbindin gene 43 Colorectal cancer 43 Leber hereditary optic neuropathy 43 Guillain Barre 43 TACI mutations 43 Porphyria 43 familial adenomatous polyposis FAP 43 basal cell carcinomas 43 Pancreatic Cancer 43 nonhereditary 43 ischemic colitis 43 BRAF gene 43 infantile autism 43 blood clotting disorder 43 Glioblastoma multiforme GBM 43 FGFR2 gene 43 G6PD deficiency 43 Pulmonary Fibrosis 43 shortened telomeres 43 ALZHEIMER 'S CARE 43 Meningococcal disease 43 Vitamin D insufficiency 43 dysthymic disorder 43 placenta praevia 43 PIDD 43 autoimmune thyroid 43 neural tube defects 43 cerebral vascular disease 43 lysosomal storage disease 43 apolipoprotein E gene 43 Lisa Mosconi 43 SCA5 43 dystrophy 43 Restless Legs Syndrome 43 associated tremor ataxia 43 cervical cancer 43 presymptomatic 43 hereditary spastic paraplegia 43 Infant botulism 43 illness 43 Shy Drager syndrome 43 encephalitis meningitis 43 beta thalassemia 43 FASD 43 ciliopathies 43 Rhabdomyosarcoma 43 Cystinosis 43 Vitamin D deficiency 43 chronic illness 43 ADHD 43 Anxiety disorders 43 preterm delivery 43 Myelodysplastic syndromes 43 preterm births 43 pneumococcal pneumonia 43 CHD7 43 Vitamin B# deficiency 43 osteopenia 43 attention-deficit/hyperactivity disorder ADHD 43 herpes zoster 43 Autism Spectrum Disorder ASD 43 recessive mutations 43 chronic degenerative 43 euthymic patients 43 Tourette Syndrome TS 43 Sudden infant 43 Rubinstein Taybi syndrome 43 kernicterus 43 nonalcoholic cirrhosis 43 exfoliation glaucoma 43 Lou Gehrig Disease 43 fatal neurodegenerative disorders 43 Ankylosing spondylitis 43 Charcot Marie Tooth 43 pneumococcal infections 43 IKZF1 43 undiagnosed celiac disease 43 related maculopathy 43 chromosomal aberration 43 BRCA2 mutations 43 Dyslexia 43 alveolar rhabdomyosarcoma 43 chronic degenerative neurological 43 IL#R 43 hypophosphatasia 43 Breast cancer 43 progressive degenerative neurological 43 unprovoked seizures 43 recurrent miscarriage 43 breast cancer genes BRCA1 43 Dilated cardiomyopathy 43 Myotonic dystrophy 43 lung disease 43 prostate adenocarcinoma 43 acute rheumatic fever 43 Autism 43 Esophageal cancer 43 Obsessive compulsive disorder 43 Multiple sclerosis affects 43 Postpartum Depression 43 impaired cognition 43 hematologic disorders 43 neurological degeneration 43 blastoma 43 prematurity ROP 43 MLH1 43 BRCA2 genes 43 CNTNAP2 gene 43 familial AF 43 MELAS 43 anovulatory infertility 43 antigen PSA 43 EoE 43 prostate carcinogenesis 43 syringomyelia 43 BRCA1 mutation 43 Bladder cancer 43 tuberous sclerosis 43 gestational diabetes mellitus 43 Niemann Pick Disease 43 premature menopause 43 repeat allele 43 coronary thrombosis 43 amyloid pathology 43 Coronary artery disease 43 Metastatic melanoma 43 Deep vein thrombosis 43 smoldering myeloma 43 Polymorphic Ventricular Tachycardia CPVT 43 faulty BRCA2 gene 43 Tay Sachs Disease 43 CNVs 43 anorexia nervosa 43 latent TB infection 43 hereditary blindness 43 herpes encephalitis 43 prostate tumors 43 Proteus syndrome 43 Postpartum psychosis 43 postnatal depression 43 psychiatric illnesses 43 Arnold Chiari Malformation 43 primary biliary cirrhosis 43 recessive genetic 43 PTPN# 43 nephritis 43 vitamin B# deficiency 43 Duchenne Muscular Dystrophy 43 Perthes disease 43 spontaneous preterm delivery 43 LHON 43 atherothrombotic disease 43 PTEN mutations 43 anterograde amnesia 43 neurodevelopmental disability 43 mutations 43 vascular cognitive impairment 43 depressive disorders 43 anencephaly 43 DiGeorge syndrome 43 brain atrophy 43 Nephrogenic Systemic Fibrosis NSF 43 neuroblastomas 43 G#S [002] 43 Prediabetes 42 Schizophrenia affects 42 BRCA1 gene mutation 42 Myelodysplastic syndromes MDS 42 motor neuron degeneration 42 Tardive dyskinesia 42 GM1 gangliosidosis 42 brain tumor 42 embryonal rhabdomyosarcoma 42 spontaneous preterm birth 42 rotavirus infections 42 Progressive Supranuclear Palsy 42 neurodegeneration 42 dysbindin 42 toxoplasmosis 42 Lou Gehrigs disease 42 congenital deafness 42 apoE4 42 TMEM#B 42 lipid disorders 42 acute lymphoid leukemia 42 cardiac hypertrophy 42 metabolic disorder 42 Chronic fatigue