Related by context. All words. (Click for frequent words.) 72 Tay Sachs disease 59 familial dysautonomia 59 Fragile X 58 Fanconi anemia 56 Familial Dysautonomia 56 Neurofibromatosis 56 Ashkenazi Jews 56 genetic disorders 56 Tay Sachs Disease 56 cystic fibrosis 55 Spinal Muscular Atrophy 55 Krabbe Disease 55 genetic defects 55 holoprosencephaly 55 mitochondrial disease 55 thalassemia 55 Tuberous Sclerosis 54 spinal muscular atrophy 54 Canavan Disease 54 Fragile X Syndrome 54 DiGeorge Syndrome 54 Hemochromatosis 54 chromosomal defect 54 Dravet syndrome 54 Niemann Pick 54 Ashkenazi Jewish 54 leukodystrophies 54 Retinoblastoma 54 CHARGE syndrome 54 Diamond Blackfan anemia 54 Spinal Muscular Atrophy SMA 54 neuroblastoma 54 histiocytosis 54 Osteosarcoma 53 HNPCC 53 Fanconi Anemia 53 mitochondrial disorders 53 APOL1 53 MYH9 gene 53 autosomal recessive disease 53 hereditary diseases 53 beta thalassemia 53 toxoplasmosis 53 hereditary deafness 53 Niemann Pick disease 53 genetic disorder 53 Acute Myelogenous Leukemia 52 Porphyria 52 fatal neuromuscular disorder 52 Meckel Gruber 52 genetic abnormality 52 Krabbe disease 52 ataxia telangiectasia 52 Tuberous Sclerosis Complex 52 familial adenomatous polyposis 52 Polycystic Kidney Disease 52 Prader Willi syndrome 52 Hurler syndrome 52 leukemia 52 autosomal recessive 52 MCAD deficiency 52 Fanconi anemia rare 52 spinal muscular atrophy SMA 52 Lafora disease 52 chromosome abnormality 51 Cystic Fibrosis 51 Newborn screening 51 biliary atresia rare 51 genetic abnormalities 51 Rett Syndrome 51 Trisomy 51 LQTS 51 Leukodystrophy 51 Spina bifida 51 galactosemia 51 Usher Syndrome 51 Kufs disease 51 Severe Combined Immunodeficiency 51 Cytomegalovirus 51 degenerative neuromuscular disease 51 Langerhans cell histiocytosis 51 systemic scleroderma 51 fatal neurodegenerative 51 lymphoblastic lymphoma 51 primary immunodeficiency 51 recessive gene 51 leukodystrophy 51 Von Hippel Lindau 51 JMML 51 Brugada Syndrome 51 prenatal diagnosis 51 Angelman Syndrome 51 Medulloblastoma 50 degenerative disorder 50 biliary atresia 50 retinoblastoma 50 Alport Syndrome 50 juvenile diabetes 50 Diamond Blackfan Anemia 50 Pompe Disease 50 neurofibromatosis 50 BRCA 50 chromosomal disorders 50 recessive mutations 50 disease 50 chromosomal disorder 50 hypophosphatasia 50 osteogenesis imperfecta 50 Sanfilippo Syndrome 50 carcinoid cancer 50 Gaucher disease 50 juvenile myelomonocytic leukemia 50 DiGeorge syndrome 50 Fragile X gene 50 bone marrow transplants 50 genetic defect 50 Diffuse Intrinsic Pontine Glioma 50 Sturge Weber 50 Wilms tumor 50 gene mutations 50 Hutchinson Gilford Progeria 50 Niemann Pick Disease 50 Cholangiocarcinoma 50 Dravet Syndrome 50 sickle cell disease 50 hemochromatosis 50 Joubert Syndrome 50 Beckwith Wiedemann syndrome 50 Down syndrome 50 Becker muscular dystrophy 50 familial ALS 50 mutated gene 50 Adrenoleukodystrophy 50 Spinal muscular atrophy 50 Prematurity 49 Retinopathy 49 degenerative neurological disorder 49 hemophagocytic lymphohistiocytosis 49 Muscular dystrophy 49 Inflammatory Breast Cancer 49 Usher syndrome 49 MCADD 49 latent TB 49 hereditary disorder 49 defective gene 49 mosaicism 49 BRCA gene 49 Pulmonary Fibrosis 49 chordoma 49 fatal neurodegenerative disorder 49 CdLS 49 genetic syndromes 49 NF1 49 neurofibromatosis type 49 myelodysplasia 49 latent tuberculosis 49 incurable genetic 49 Aplastic Anemia 49 Wiskott Aldrich Syndrome 49 mitochondrial diseases 49 Toxoplasmosis 49 incurable neurological disorder 49 epidermolysis bullosa EB 49 Smith Lemli Opitz 49 Hepatitis B virus 49 sickle cell anemia 49 Anencephaly 49 pneumococcal meningitis 49 Cystinosis 49 tuberous sclerosis complex 49 Rhabdomyosarcoma 49 Neuroblastoma 49 myeloproliferative neoplasms 49 Sickle Cell Anemia 49 Chronic lymphocytic leukemia 49 Cystic fibrosis 49 Hirschsprung disease 49 dominantly inherited 49 Angelman 49 DIPG 49 Aplastic anemia 49 Necrotizing Fasciitis 49 BRCA mutations 49 Scleroderma 49 G#S mutation 49 mutation 49 Wiskott Aldrich syndrome 49 epidermolysis bullosa 49 NF2 48 neurodegenerative disorder 48 gene mutation 48 acute lymphoid leukemia 48 Batten Disease 48 ectodermal dysplasia 48 Crigler Najjar syndrome 48 Apert syndrome 48 Primary Immune Deficiency 48 hereditary disorders 48 Acute myeloid leukemia 48 Mitochondrial Disease 48 hemolytic anemia 48 Wilm tumor 48 Li Fraumeni syndrome 48 Wilms Tumor 48 Krabbe leukodystrophy 48 Sanfilippo syndrome 48 Krabbe Leukodystrophy 48 Leber congenital amaurosis 48 Langerhans Cell Histiocytosis 48 acute myeloid leukemia 48 Cockayne syndrome 48 severe aplastic anemia 48 Fragile X. 48 germline mutations 48 Huntington Disease 48 colorectal cancer CRC 48 myotonic dystrophy 48 Moyamoya disease 48 G6PD deficiency 48 Acute Lymphoblastic Leukemia 48 recessive genetic 48 TTTS 48 Acute Respiratory Failure 48 metabolic disorder 48 Hemophilia B 48 Lou Gehrigs disease 48 VCFS 48 chromosomal anomaly 48 Angelman syndrome 48 inherited neurodegenerative disorder 48 paralytic polio 48 rare chromosomal disorder 48 Alagille syndrome 48 hereditary predisposition 48 BRCA genes 48 Genetic Disorders 48 congenital disorders 48 strep bacteria 48 thrombophilia 48 Marfan 48 variable immunodeficiency 48 congenital hypothyroidism 48 CHDs 48 Friedreich ataxia 48 Rett syndrome 48 recessively inherited 48 Leber Congenital Amaurosis 48 neurodegenerative disease 48 spinal muscle atrophy 48 Celiac sprue 48 chromosomal abnormality 48 Haemophilia 48 Sickle cell 48 Spina Bifida 48 Primary Immunodeficiency 48 tuberous sclerosis 48 sickle cell 48 HIBM 48 cystic fibrosis Duchenne muscular 48 Sandhoff disease 48 immunodeficiency disease 48 chromosomal defects 48 smoldering myeloma 47 phenylketonuria 47 ARVD 47 Babesiosis 47 Smith Lemli Opitz syndrome 47 infantile spasms 47 Herpes simplex virus 47 hereditary nonpolyposis colorectal cancer 47 anencephaly 47 prion disease 47 Noonan Syndrome 47 Hypoplastic Left Heart 47 Meningococcal Meningitis 47 B strep 47 progressive neurological disorder 47 Polycystic kidney disease 47 autism neurological disorder 47 Duchenne 47 immunodeficiency disorder 47 FSGS 47 Alport syndrome 47 disorder thalassemia 47 aplastic anemia 47 V Leiden 47 Joubert syndrome 47 herpesviruses 47 Thalassemia 47 maternally inherited 47 Fragile X syndrome 47 muscular dystrophy cystic fibrosis 47 gene BRCA2 47 Rhabdomyosarcoma rare 47 Childhood Disorder 47 unexplained mental retardation 47 Von Willebrand disease 47 CHARGE Syndrome 47 Epstein Barr Virus 47 AAT deficiency 47 spontaneous mutations 47 neurofibromatosis genetic disorder 47 MSH2 47 1 Antitrypsin Deficiency 47 Hypophosphatasia 47 Newborn Screening 47 mitochondrial myopathy 47 Down Syndrome 47 Histiocytosis 47 lupus 47 Genetic Disease 47 autoinflammatory diseases 47 Cystic Fibrosis CF 47 diaphragmatic hernia 47 monogenic diabetes 47 Glioblastoma 47 transverse myelitis 47 cystic fibrosis hereditary 47 APOE gene 47 BRCA mutation 47 Beta thalassemia 47 cystic fibrosis CF 47 BRCA1 mutations 47 hypertrophic cardiomyopathy HCM 47 Ehlers Danlos 47 familial pancreatic cancer 47 ApoE4 gene 47 aneuploidies 47 frontotemporal dementia 47 implantation genetic 47 diffuse intrinsic pontine glioma 47 lymphangioleiomyomatosis LAM 47 trisomy 47 acute lymphoblastic leukemia 47 HHV 6 47 Down syndrome spina bifida 47 vWD 47 Leber congenital amaurosis LCA 47 cystic fibrosis sickle cell 47 BRCA1 gene 47 Leukemia 47 congenital deafness 47 Acute Leukemia 47 heritable genetic 47 Wilm Tumor 47 Amyotrophic lateral sclerosis ALS 47 oligodendrogliomas 47 Kawasaki Disease 47 choriocarcinoma 46 inherited neurological disorder 46 chronic granulomatous disease 46 Hermansky Pudlak Syndrome 46 Acute Promyelocytic Leukemia 46 acute lymphatic leukemia 46 strep 46 mastocytosis 46 autosomal recessive disorder 46 hepatoblastoma 46 Celiac disease 46 cysticercosis 46 Acute lymphoblastic leukemia 46 Pancreatic 46 fungal meningitis 46 PIDD 46 Down syndrome chromosomal disorder 46 Levy Lahad 46 Burkitt Lymphoma 46 acute leukemias 46 Pneumococcal meningitis 46 Arrhythmogenic Right Ventricular Cardiomyopathy 46 Inflammatory Bowel Disease 46 genetic mutations 46 Joubert syndromes 46 Retinitis pigmentosa 46 Lymphoma 46 Cryptococcus neoformans 46 mitochondrial dysfunction 46 hereditary hemochromatosis 46 Aicardi syndrome 46 genetically inherited 46 APOE4 46 Polymorphic Ventricular Tachycardia CPVT 46 myositis 46 HGPS 46 Carcinoid 46 frontal temporal dementia 46 Rh positive 46 rhabdomyosarcoma 46 Progeria 46 hereditary spastic paraplegia 46 Aneuploidy 46 cause cardiac channelopathies 46 Idiopathic Thrombocytopenic Purpura ITP 46 medulloblastoma tumors 46 Mitochondrial diseases 46 Duchenne Muscular Dystrophy 46 Congenital Adrenal Hyperplasia 46 bicuspid valve 46 fronto temporal dementia 46 autoinflammatory 46 Leber Congenital Amaurosis LCA 46 PTLD 46 de novo mutations 46 atypical rhabdoid tumor 46 • LI Tourette 46 Lou Gerhig disease 46 dyskeratosis congenita 46 Fanconi 46 Hodgkin Disease 46 molybdenum cofactor deficiency 46 degenerative nerve disorder 46 leukemia ALL 46 Acute Lymphocytic Leukemia 46 Leukemias 46 chromosomal abnormalities 46 lymphoblastic leukemia 46 genetic mutation 46 surrogacies 46 Cushing syndrome 46 recessive trait 46 prenatally diagnosed 46 TACI mutations 46 Hutchinson Gilford Progeria Syndrome 46 Pompe disease rare 46 Rh incompatibility 46 fibrodysplasia ossificans progressiva FOP 46 BRCA1 46 MELAS 46 Duchenne muscular dystrophy 46 systemic mastocytosis 46 vasa previa 46 autism 46 Myositis 46 Hurler Syndrome 46 Autoimmune disorders 46 chlamydial infections 46 neuroblastomas 46 Respiratory Syncytial Virus RSV 46 Human Papillomavirus 46 Dystonia 46 juvenile dermatomyositis 46 1 diabetes T1D 46 Genital herpes 46 thoracic aortic disease 46 acute myelogenous leukemia AML 46 mitochondrial mutations 46 newborn screening 46 Aicardi Syndrome 46 chronic autoimmune disorder 46 brain malformation 46 microdeletion 46 neurogenetic 46 auditory neuropathy 46 severe congenital neutropenia 46 spinocerebellar ataxia 46 Parkinson disease neurodegenerative disorder 46 Bronchiolitis 46 Lewy Body Dementia 46 ADA SCID 46 Marfan Syndrome 46 Duchenne Muscular Dystrophy DMD 45 neuromuscular disease 45 Hashimoto thyroiditis 45 Fatty Liver Disease 45 antibiotic resistant bacterial infection 45 homozygous FH 45 AAT Deficiency 45 breast carcinomas 45 Alzheimer 45 kidney disease 45 Myasthenia gravis 45 marrow transplant 45 diagnosed prenatally 45 myelomeningocele 45 PGD 45 chromosome abnormalities 45 Glioblastoma multiforme GBM 45 interferon pathway 45 inherited retinal degeneration 45 neuro degenerative disease 45 lysosomal storage diseases 45 cystinosis 45 IgA deficiency 45 Arnold Chiari 45 onset Alzheimer disease 45 inherited mutations 45 Sudden Arrhythmia Death 45 preimplantation genetic diagnosis 45 spontaneous remission 45 Progressive Supranuclear Palsy 45 progressive neurodegenerative disorder 45 celiac 45 neuroblastoma tumor 45 Crohns Disease 45 Lou Gherig Disease 45 Myopathy 45 Myocarditis 45 Hereditary angioedema HAE 45 diseases 45 MDR tuberculosis 45 sporadic CJD 45 Tay Sachs thalassemia 45 inherited neurodegenerative 45 metachromatic leukodystrophy 45 ApoE gene 45 causative gene 45 myasthenia gravis neuromuscular 45 CMV infection 45 ADPKD 45 latent TB infection 45 cryptococcal meningitis 45 lysosomal diseases 45 metastatic cancer 45 deafness neurological 45 Rubinstein Taybi syndrome 45 Nonalcoholic fatty liver 45 XMRV infection 45 Myasthenia 45 adrenoleukodystrophy ALD 45 myelodysplastic syndrome 45 Prader Willi 45 Creutzfeldt Jakob Disease 45 Chronic Rhinosinusitis 45 sickle cell cystic fibrosis 45 secretory diarrhea 45 HLA identical 45 Kleine Levin 45 anencephaly fatal 45 Celiac 45 autism spectrum disorders 45 lactose malabsorption 45 genes BRCA1 45 congenital muscular dystrophy 45 mutations 45 liver disease 45 Hutchinson Gilford progeria 45 craniosynostosis 45 alveolar rhabdomyosarcoma 45 basal cell nevus syndrome 45 RhD negative 45 nonhereditary 45 celiac disease 45 pneumococci 45 neurodermatitis 45 Biliary atresia 45 Creutzfeldt Jakob 45 neurological disorder 45 hereditary blindness 45 Alzheimer Dementia 45 Gaucher Disease 45 cardiac channelopathies 45 Pelizaeus Merzbacher disease 45 congenital CMV 45 Barth Syndrome 45 precocious puberty 45 multiforme 45 Dravet 45 Epidermolysis bullosa 45 Chagas disease 45 congenital adrenal hyperplasia CAH 45 carcinoid tumor 45 Coeliac disease 45 Hemolytic Uremic Syndrome 45 haemochromatosis 45 medium chain acyl 45 invasive secretory carcinoma 45 CIDP 45 acute myelogenous leukemia 45 degenerative neurological disease 45 BRCA2 mutations 45 inheritable diseases 45 testicular cancers 45 Crohn 45 Severe Primary IGFD 45 kernicterus 45 rheumatic disease 45 achondroplasia 45 monozygotic twin 45 Lyme Disease 45 renovascular hypertension 45 type 1diabetes 45 NTDs 45 polycystic ovary syndrome 45 Hirschsprung Disease 45 Motor neurone disease 45 NOMID 45 Ewings Sarcoma 45 Chronic Inflammatory Demyelinating Polyneuropathy 45 Lewy Body 45 Ataxia 45 Lymphomas 45 leukemias 45 genetic lysosomal storage 45 Sickle Cell 45 synovial sarcoma 45 ceroid lipofuscinosis NCL 44 medulloblastoma 44 Trichomonas 44 Prion diseases 44 Osteogenesis Imperfecta 44 FMR1 gene 44 CHD7 44 glioblastoma 44 Mendelian disorders 44 pseudotumor cerebri 44 Beta Thalassemia 44 primary immunodeficiencies 44 congenital rubella syndrome 44 Cystic fibrosis CF 44 debilitating neurological disorder 44 Duchenne muscular dystrophy DMD 44 recessive genes 44 cystic fibrosis chronic pancreatitis 44 scleroderma 44 Neurofibromatosis type 44 mutant gene 44 sCJD 44 thyroiditis 44 Treacher Collins 44 Maroteaux Lamy syndrome 44 herpes viruses 44 chromosomal anomalies 44 familial adenomatous polyposis FAP 44 uterus didelphys 44 Waldenstrom macroglobulinemia 44 Burkitt lymphoma 44 parasitic infections 44 achromatopsia 44 Lou Gherig disease 44 primary sclerosing cholangitis 44 juvenile idiopathic arthritis JIA 44 neuro muscular diseases 44 Autism Spectrum Disorder 44 aneuploidy 44 SCID 44 immunodeficiency 44 Cooley Anemia 44 cancers 44 X SCID 44 Chronic Lymphocytic Leukemia 44 breast cancer genes BRCA1 44 Alzhiemer 44 unexplained infertility 44 Ewing sarcoma 44 Carcinoid tumors 44 deleterious mutation 44 Acute Lymphoblastic Leukaemia 44 combined immunodeficiency SCID 44 streptococcal infection 44 acute lymphocytic leukemia 44 deletion 5q 44 autosomal recessive genetic 44 neuro degenerative disorder 44 ovarian cancer 44 immunocompetent 44 Sarcoidosis 44 variant CJD 44 osteopetrosis 44 familial hypercholesterolaemia 44 SADS 44 Chlamydia trachomatis 44 ovarian tumors 44 Dysautonomia 44 lymphocytic choriomeningitis virus 44 2 diabetes T2D 44 Primary immunodeficiency 44 neuroendocrine tumors 44 Hydrocephalus 44 cystic fibrosis muscular dystrophy 44 GPC5 44 Variant CJD 44 molar pregnancy 44 chronic lymphocytic 44 hemolytic uremic syndrome HUS 44 Hib meningitis 44 Jeffrey Modell 44 neuroendocrine cancers 44 progressive supranuclear palsy 44 Premature birth 44 ichthyosis 44 PNET 44 Sturge Weber syndrome 44 diagnosis PGD 44 Thalassaemia 44 Wegener granulomatosis 44 Myelodysplastic syndrome 44 leukaemias 44 Fanconi anemia FA 44 Malignancies 44 Ichthyosis 44 Epstein Barr virus EBV 44 Preeclampsia 44 malignant hyperthermia 44 Infertility 44 HLA markers 44 Juvenile Arthritis 44 measles virus 44 Cytomegalovirus CMV 44 progressive neurodegenerative disease 44 infantile hemangiomas 44 GIST tumors 44 Graft Versus Host 44 Chronic myeloid leukemia CML 44 roseola 44 Epstein Barr 44 Inflammatory bowel diseases 44 Congenital Heart Defects 44 myotonic muscular dystrophy 44 immunodeficiencies 44 Myelodysplastic Syndrome 44 Alzheimers Disease 44 Amyotrophic lateral sclerosis 44 prion diseases 44 neurodevelopmental disorders 44 Herpes Simplex Virus 44 mutated BRCA 44 cancerdefine 44 Glioblastoma Multiforme GBM 44 Juvenile Rheumatoid Arthritis 44 herpes infection 44 hereditary breast cancer 44 Acute Myeloid Leukemia 44 BRCA1 gene mutation 44 JAK mutations 44 Eosinophilic 44 polycystic kidney disease 44 Soft Tissue Sarcoma 44 leukemia lymphoma myeloma 44 Myelodysplastic syndromes 44 Duchenne Becker 44 Moebius syndrome 44 pancreases 44 Combined Immune Deficiency 44 cytomegalovirus 44 Wilms Tumour 44 acute lymphoblastic 44 Apert 44 combined immunodeficiency 44 chromosomal rearrangements 44 hemolytic disease 44 leukemia lymphoma 44 Herpes 44 Duchene muscular dystrophy 44 streptococcal 44 necrotizing enterocolitis NEC 44 Tourette Syndrome TS 44 juvenile rheumatoid arthritis 44 islet transplants 44 amyotrophic lateral sclerosis ALS 44 pleural mesothelioma 44 lymphocytic leukemia 44 Sjogren Syndrome 44 Pemphigus 44 incurable neurodegenerative disease 44 diabetes 44 Salmonella serotype 44 Brittle Bone 44 MPGN 44 Pseudomonas infections 44 Bronchiectasis 44 childhood leukemia 44 Patau syndrome 44 dermatofibrosarcoma protuberans 44 TTR amyloidosis 44 leukemia lymphoma multiple myeloma 44 Pre eclampsia 44 myelodysplastic syndrome MDS 44 Guillain Barré Syndrome 44 Childhood Diseases 44 Lymphoproliferative 44 neonatal herpes 44 skeletal dysplasia 44 bacterium Staphylococcus aureus 44 acute myeloid 44 blastoma 44 appendiceal cancer 44 muscular dystrophy 44 Lateral Sclerosis 44 BRAF gene 44 prostate adenocarcinoma 44 muscular dystrophies 44 celiac sprue 44 Retinitis Pigmentosa RP 44 Human Papillomavirus HPV 44 Glycogen Storage Disease 44 embryonal rhabdomyosarcoma 43 Crohn disease 43 Moyamoya 43 Myotonic dystrophy 43 mycobacterium tuberculosis 43 Reflex Sympathetic Dystrophy Syndrome 43 rubella 43 hyperemesis gravidarum 43 Proteus syndrome 43 Kurtzberg 43 simplex virus 43 human leukocyte antigen 43 immune deficiency 43 neuropsychiatric disorder 43 myasthenia gravis MG 43 LRRK2 gene 43 polycystic ovarian syndrome PCOS 43 acute myelocytic leukemia 43 nephrosis 43 Cardiomyopathy 43 autosomal dominant polycystic kidney 43 Sporadic CJD 43 Gliomas 43 neoplastic diseases 43 mutated genes 43 Long QT Syndrome 43 Beckwith Wiedemann Syndrome 43 Haptoglobin 43 apolipoprotein E gene 43 Morquio syndrome 43 Scoliosis 43 HELLP syndrome 43 Testicular Cancer 43 heartworms 43 Congenital heart 43 FXTAS 43 primary biliary cirrhosis 43 recessive inheritance 43 Guillain Barre Syndrome 43 amyloidosis 43 IL#R 43 ataxias 43 lissencephaly 43 autoimmune disease 43 mental retardation epilepsy 43 Sarcoma 43 Liver Disease 43 congenital toxoplasmosis 43 hematologic disorders 43 Alzeimer 43 ataxia telangiectasia AT 43 cancer 43 anemias 43 Brain Tumor 43 fatty liver disease 43 HLH 43 IVF embryos 43 PTEN mutations 43 Merkel Cell Carcinoma 43 paraganglioma 43 angiosarcoma 43 Fanconi Anaemia 43 gestational diabetes mellitus 43 gastrointestinal stromal tumor 43 congenital blindness 43 spina bifida 43 spastic diplegia 43 PDGFRA 43 Ewing sarcoma rare 43 cardiovascular restenosis cancer 43 gluten intolerance 43 ApoE4 allele 43 Ebola Hemorrhagic Fever 43 PANDAS 43 RDEB 43 multidrug resistant strains 43 Melanoma 43 ependymoma 43 Treacher Collins syndrome 43 ARVC 43 colon cancers 43 incurable hereditary 43 Crouzon Syndrome 43 Alzheimers disease 43 encephalitis swelling 43 intractable epilepsy 43 RhD 43 Dwarfism 43 Cockayne Syndrome 43 Klinefelter Syndrome 43 streptococcal infections 43 Friedreich Ataxia 43 RPE# 43 Dysplasia 43 Churg Strauss syndrome 43 Pulmonary arterial hypertension 43 myalgic encephalomyelitis ME 43 progressive multifocal PML 43 chromosome deletion 43 diffuse gastric 43 Glioblastoma Multiforme 43 toxemia 43 limb girdle muscular dystrophy 43 VZV 43 pharyngeal cancer 43 genetic neuromuscular disorder 43 narcolepsy cataplexy 43 Premature Ovarian Failure 43 Stargardt macular dystrophy 43 Holoprosencephaly 43 Fibrodysplasia 43 congenital hydrocephalus 43 CJD 43 idiopathic epilepsy 43 autosomal dominant disorder 43 Malignant gliomas 43 progressive neuromuscular 43 Wegener Granulomatosis 43 teratoma 43 Acute Renal Failure 43 Pancreatic Cancer 43 neurodevelopment disorder 43 mental retardation blindness 43 nasopharyngeal carcinoma NPC 43 epilepsies 43 Non Hodgkin 43 autism spectrum disorder 43 congenital anomalies 43 lysosomal storage disease 43 GISTs 43 polydactylism 43 Leber hereditary optic neuropathy 43 disease epidermolysis bullosa 43 Acute lymphocytic leukemia 43 Lupus 43 tick borne disease 43 Fraternal twins 43 idiopathic pulmonary fibrosis 43 Respiratory Syncytial Virus 43 Chronic Myelogenous Leukemia 43 Reactive Attachment Disorder 43 thymic carcinoma 43 Vasculitis 43 congenital diaphragmatic hernia 43 #q#.# deletion syndrome 43 Helicobacter pylori infection 43 compulsive hoarding 43 Ulcerative Colitis 43 Mantle Cell Lymphoma 43 HLA B# 43 Shy Drager syndrome 43 preimplantation genetic diagnosis PGD 43 progressive neurodegenerative 43 chronic rheumatic 43 Hurthle cell 43 twin transfusion 43 Fibromyalgia Chronic Fatigue Syndrome 43 Dystrophy 43 VUR 43 hydrops 43 Creutzfeldt Jakob disease 43 PDD NOS 43 Hepatitis B 43 Bloodstream infections 43 untreated celiac disease 43 malformation 43 Goldenhar syndrome 43 primitive neuroectodermal tumor 43 Anaplastic 43 hormonal disorder 43 bone marrow transplant 43 congenital heart 43 Parvo 43 Klinefelter syndrome 43 inappropriate antidiuretic hormone SIADH 43 malignancy 43 ALS 43 Hodgkins Lymphoma 43 Hydrocephalus Foundation 43 Urea Cycle Disorders 43 Transverse Myelitis 43 HbF 43 autoimmune 43 familial hypercholesterolemia 43 endometrial cancers 43 Duchene Muscular Dystrophy 43 Myasthenia Gravis Foundation 43 autosomal dominant 43 Syndrome 43 Polycystic Ovary Syndrome 43 congenital hemophilia 43 Syringomyelia 43 EoE 43 essential thrombocythemia 43 Alzheimer disease AD 43 FEVR 43 CFTR gene 43 epigenetic alterations 43 Raynaud disease 42 myelogenous leukemia 42 Guillain Barr 42 hypereosinophilic syndrome 42 Pervasive Developmental Disorder 42 Crohns 42 Scleroderma Research 42 haemophilia 42 Necrotizing fasciitis 42 leukemic 42 APOE ε4 42 PPCM 42 curable cancers 42 Sickle Cell Disease 42 Juvenile Idiopathic Arthritis JIA 42 Cerebral palsy