Related by context. All words. (Click for frequent words.) 72 Progeria 66 progeria rare 59 HGPS 58 Rett syndrome 58 mitochondrial disease 57 Hutchinson Gilford Progeria 56 Fanconi anemia 56 Angelman Syndrome 56 spinal muscular atrophy SMA 56 genetic disorder 55 neuroblastoma 55 Angelman syndrome 55 Friedreich ataxia 54 Leber congenital amaurosis 54 mitochondrial diseases 54 Hutchinson Gilford Progeria Syndrome 54 neurofibromatosis 54 Duchenne Muscular Dystrophy 54 degenerative disorder 54 Duchenne 54 Duchenne muscular dystrophy 54 Usher Syndrome 54 mitochondrial dysfunction 54 retinoblastoma 53 sickle cell disease 53 polycystic kidney disease 53 NF2 53 muscular dystrophy 53 DiGeorge Syndrome 53 Rett Syndrome 53 medulloblastoma 53 Leber congenital amaurosis LCA 53 lymphoblastic leukemia 53 myotonic dystrophy 53 autism spectrum disorders 52 Spinal Muscular Atrophy SMA 52 Sanfilippo syndrome 52 acute myelogenous leukemia AML 52 NF1 52 Sanfilippo Syndrome 52 rhabdomyosarcoma 52 acute myeloid leukemia 52 Pompe Disease 51 Usher syndrome 51 leukemia 51 Leber Congenital Amaurosis LCA 51 Dravet syndrome 51 medulloblastomas 51 Spinal Muscular Atrophy 51 dyskeratosis congenita 51 FSGS 51 acute myelogenous leukemia 51 Fragile X syndrome 51 beta thalassemia 51 cystic fibrosis 51 Duchenne muscular dystrophy DMD 51 Retinoblastoma 51 genetic defect 51 Hutchinson Gilford progeria 51 fatal neuromuscular disorder 51 Hurler syndrome 51 neurodegenerative disease 50 inherited neurodegenerative disorder 50 Alzheimers disease 50 Niemann Pick disease 50 chromosomal defect 50 severe aplastic anemia 50 retinal degeneration 50 Progeria Research 50 Muscular dystrophy 50 Duchenne Muscular Dystrophy DMD 50 biliary atresia 50 neurodegenerative disorder 50 chromosomal disorder 50 degenerative neurological disorder 50 Alzheimer disease AD 50 ataxia telangiectasia 50 autism spectrum disorder 50 Joubert syndrome 50 Fragile X Syndrome 50 Niemann Pick 50 neurodegeneration 50 dilated cardiomyopathy 50 lymphoblastic lymphoma 50 Alzheimer 49 neuroblastomas 49 Alzheimer disease 49 FTLD 49 cystic fibrosis CF 49 RDEB 49 incurable genetic 49 fatal neurodegenerative disorder 49 DiGeorge syndrome 49 chromosome abnormality 49 leukemia ALL 49 pseudotumor cerebri 49 metabolic disorder 49 Cardiomyopathy 49 Rhabdomyosarcoma 49 Krabbe disease 49 hypothalamic hamartoma 49 nonsense mutation 49 ependymoma 49 genetic abnormality 49 retinitis pigmentosa 49 Krabbe Disease 49 renovascular hypertension 49 congenital heart 49 galactosemia 49 Wilms tumor 49 congenital muscular dystrophy 48 mutated genes 48 Aspergers syndrome 48 diffuse intrinsic pontine glioma 48 fatty liver disease 48 autoimmune encephalitis 48 scoliosis 48 Fanconi Anemia 48 hypophosphatasia 48 Marfan syndrome 48 sporadic ALS 48 Hirschsprung disease 48 congenital blindness 48 lysosomal storage diseases 48 eosinophilic esophagitis 48 degenerative neurological disease 48 Neuroblastoma 48 Retinopathy 48 spinocerebellar ataxia 48 glioblastoma 48 inherited neurological disorder 48 Becker muscular dystrophy 48 mutations 48 epidermolysis bullosa EB 48 diffuse pontine glioma 48 Alzheimer Disease 48 wet macular degeneration 48 brain malformation 48 carcinoid cancer 48 ARVD 48 Fragile X. 48 Proteus Syndrome 48 histiocytosis 48 achromatopsia 48 neurological disorder 48 ectodermal dysplasia 47 inherited retinal degeneration 47 neurodegenerative disorders 47 lupus 47 neurodegenerative 47 familial adenomatous polyposis 47 autosomal dominant 47 Kufs disease 47 Medulloblastoma 47 prion diseases 47 medulloblastoma tumors 47 Peutz Jeghers syndrome 47 congenital deafness 47 Burkitt lymphoma 47 spinal muscular atrophy 47 autism 47 Leber Congenital Amaurosis 47 mitochondrial disorders 47 genetic abnormalities 47 fibrodysplasia ossificans progressiva FOP 47 MCAD deficiency 47 motor neuron disease 47 cardiac hypertrophy 47 Osteosarcoma 47 tuberous sclerosis complex 47 hypertrichosis 47 genetic mutation 47 Histiocytosis 47 Fanconi anemia rare 47 DIPG 47 Maroteaux Lamy Syndrome 47 G#S mutation 47 progressive neurological disorder 47 neuromuscular disease 47 Marfan 47 infantile spasms 47 familial hypercholesterolemia 47 carcinoid 47 Severe Primary IGFD 47 juvenile dermatomyositis 47 Hurler Syndrome 47 mutated gene 47 immunodeficiency disorder 47 Acute Lymphoblastic Leukaemia 47 Autism Spectrum Disorder ASD 47 osteopetrosis 47 ASDs 47 enzyme deficiency 47 prion disease 46 Krabbe Leukodystrophy 46 Duchene muscular dystrophy 46 Lafora disease 46 atypical hemolytic uremic syndrome 46 cystinosis 46 Leber Hereditary Optic Neuropathy 46 myasthenia gravis 46 Alport syndrome 46 progressive neurodegenerative disorder 46 fatal neurodegenerative 46 epidermolysis bullosa 46 CHARGE syndrome 46 acute lymphoblastic leukemia 46 mitochondrial mutations 46 JAK mutations 46 defective gene 46 Apert syndrome 46 Pompe disease 46 incurable neurodegenerative disease 46 familial ALS 46 autoimmune 46 Chiari malformation 46 Tay Sachs disease 46 T1DM 46 chromosome deletion 46 JMML 46 Cockayne syndrome 46 thalassemia 46 LQTS 46 VCFS 46 gene mutation 46 fungal meningitis 46 dystrophy 46 leukemia AML 46 acute myeloid leukemia AML 46 myelogenous leukemia 46 Parkinsons disease 46 hereditary spastic paraplegia 46 Pompe disease rare 46 motor neurone 46 neurofibromatosis type 46 Kabuki syndrome 46 Diamond Blackfan Anemia 46 adrenoleukodystrophy ALD 46 Batten Disease 46 Retinitis Pigmentosa RP 46 TTR amyloidosis 46 Acute Myelogenous Leukemia 46 alopecia areata 46 alzheimer disease 46 synovial sarcoma 46 sickle cell 46 Sandhoff disease 46 Aicardi syndrome 46 neurodevelopmental disorders 46 juvenile diabetes 46 ALS 46 Lou Gherig disease 46 hemolytic anemia 46 RPE# 46 neuro degenerative disorder 46 Transverse Myelitis 46 fibrodysplasia ossificans progressiva 46 Severe Combined Immunodeficiency 46 iron overload 46 holoprosencephaly 46 Goldenhar syndrome 46 huntingtin gene 46 neuroblastoma tumor 45 Kawasaki Disease 45 unrepaired clefts 45 Wiskott Aldrich Syndrome 45 psychosocial dwarfism 45 limb girdle muscular dystrophy 45 diabetic retinopathy DR 45 blastoma 45 retinitis pigmentosa RP 45 congenital disorders 45 CdLS 45 protein misfolding 45 degenerative muscular 45 retinoblastoma rare 45 mastocytosis 45 Joubert Syndrome 45 genetic defects 45 alopecia 45 Alzheimer pathology 45 macular degeneration 45 obsessive compulsive disorder OCD 45 mitochondrial disorder 45 Ataxia Telangiectasia 45 osteogenesis imperfecta 45 congenital disorder 45 immunodeficiency 45 Duchene Muscular Dystrophy 45 dwarfism 45 FSHD 45 inherited neurodegenerative 45 Male pattern baldness 45 genetic mutations 45 corneal blindness 45 Wilm Tumor 45 Trisomy 45 lung fibrosis 45 autosomal recessive 45 retinal diseases 45 hereditary disorder 45 acute lymphocytic leukemia 45 hepatoblastoma 45 achondroplasia 45 Prader Willi syndrome 45 mitochondrial myopathy 45 mutation 45 ATTR PN 45 Ewing sarcoma 45 sickle cell anemia 45 Ewing Sarcoma 45 multiple myeloma 45 aplastic anemia 45 fatal neurological disorder 45 diabetic retinopathy 45 Acute Lymphoblastic Leukemia 45 Hypophosphatasia 45 Cockayne Syndrome 45 polycystic kidneys 45 LHON 45 chronic renal failure 45 dyspraxia 45 Biliary Atresia 45 sarcomas 45 Burkitt Lymphoma 45 autoimmune disease 45 Acute Myelogenous Leukemia AML 45 Mitochondrial diseases 45 cardiomyopathy 45 Synovial sarcoma 45 septo optic dysplasia 45 uncontrolled epilepsy 45 retinitis pigmentosa hereditary 45 rare chromosomal disorder 45 microcephaly 45 myeloid leukemia 45 Parkinson disease 45 type 1diabetes 45 brain tumor 45 chordoma 45 hematologic disorders 45 brain tumors 45 incurable neurological disorder 45 Aortic dissection 45 NPHP 45 bilateral retinoblastoma 45 Mitochondrial Disease 45 smoldering myeloma 44 pneumococcal meningitis 44 congenital cataract 44 Noonan Syndrome 44 Von Willebrand disease 44 breast cancer metastasis 44 Moebius Syndrome 44 pulmonary fibrosis PF 44 mtDNA mutations 44 craniosynostosis 44 leptin resistance 44 myelodysplasia 44 Lou Gerhig disease 44 cancer 44 Pompe 44 Cholangiocarcinoma 44 amyloidosis 44 immunodeficiencies 44 hypertrophic cardiomyopathy 44 precocious puberty 44 RSV infections 44 Crouzon Syndrome 44 Rubinstein Taybi syndrome 44 amyotrophic lateral sclerosis ALS 44 causative gene 44 irreversible blindness 44 Kaposi sarcoma 44 ADPKD 44 Rett syndrome neurological disorder 44 Loeys Dietz syndrome 44 juvenile myelomonocytic leukemia 44 neuropsychiatric disorder 44 muscle wasting 44 genetic disorders 44 basal cell nevus syndrome 44 neurodevelopmental disorder 44 Alzheimer Disease AD 44 cerebellar hypoplasia 44 Keratoconus 44 acute leukemia 44 juvenile idiopathic arthritis 44 autistic 44 hereditary blindness 44 muscle degeneration 44 IDH1 44 recessive genetic 44 malignant transformation 44 Alport Syndrome 44 Asperger Disorder 44 pediatric brain tumor 44 acute promyelocytic leukemia 44 motor neuron diseases 44 prematurity ROP 44 retinal dysfunction 44 familial adenomatous polyposis FAP 44 Treacher Collins syndrome 44 leukaemias 44 spastic diplegia 44 neuromuscular disorder 44 tuberous sclerosis 44 Adrenoleukodystrophy 44 DiGeorge syndrome rare 44 Down syndrome 44 genetically inherited 44 Wiskott Aldrich syndrome 44 Glioblastoma 44 compulsive hoarding 44 gene mutations 44 Alzhiemer 44 mutant protein 44 embryonal rhabdomyosarcoma 44 degenerative neuromuscular disease 44 Hodgkins Lymphoma 44 incurable neurological disease 44 cerebal palsy 44 Stargardt Macular Dystrophy 44 muscular dystrophies 44 sarcopenia 44 pemphigus 44 kidney disease 44 MSUD 44 Wilms Tumor 44 Pelizaeus Merzbacher disease 44 chronic granulomatous disease 44 mutant gene 44 Acute Leukemia 44 nonsense mutations 44 Diffuse Intrinsic Pontine Glioma 44 neurofibromatosis NF 44 Tourette syndrome neurological disorder 44 PTLD 44 tumors 44 FXTAS 44 Huntington Chorea 44 idiopathic pulmonary fibrosis IPF 44 autoimmunity 44 retinal blastoma 44 neurodegenerative diseases 44 Proteus syndrome 44 epilepsy 44 Huntington Disease 44 molecular abnormalities 44 Treacher Collins Syndrome 44 retinal degenerative disease 44 Fragile X 44 myelofibrosis 44 seizure disorders 44 hypertrophic cardiomyopathy HCM 44 Retinitis pigmentosa 44 pulmonary hypertension 44 Acute Lymphocytic Leukemia 44 Nephrotic Syndrome 43 frontotemporal dementia 43 systemic lupus erythematosus 43 Idiopathic Pulmonary Fibrosis IPF 43 AAT deficiency 43 myeloma 43 Hashimoto thyroiditis 43 degenerative diseases 43 Morquio 43 Diamond Blackfan anemia 43 blastic 43 atherosclerosis 43 biliary atresia rare 43 Polycystic Kidney Disease 43 Wegener granulomatosis 43 MELAS 43 MECP2 gene 43 hemophagocytic lymphohistiocytosis 43 Asperger 43 Long QT Syndrome 43 Hodgkin Lymphoma 43 Savant Syndrome 43 inherited metabolic disorders 43 NAFLD 43 Perthes disease 43 autosomal dominant disorder 43 related macular degeneration 43 Fragile X gene 43 Six3 43 Tourette syndrome 43 Amyotrophic lateral sclerosis ALS 43 Cystinosis 43 aHUS 43 chromosomal abnormalities 43 Langerhans cell histiocytosis 43 hereditary deafness 43 Sjögren syndrome 43 Hodgkin lymphoma 43 Niemann Pick Disease 43 lateral sclerosis 43 von Hippel Lindau 43 Cushing syndrome 43 hemochromatosis 43 sarcoma 43 immunodeficiency disease 43 Sudden Arrhythmia Death 43 Acute Myeloid Leukaemia AML 43 Guillain Barré Syndrome 43 Lorenzo Odone 43 pneumococcal pneumonia 43 fibrous dysplasia 43 Neurofibromatosis 43 MGUS 43 prostate tumors 43 neuro developmental disorder 43 leukodystrophies 43 syringomyelia 43 myoclonic epilepsy 43 Porphyria 43 Langerhans Cell Histiocytosis 43 atypical rhabdoid tumor 43 Barth Syndrome 43 NOMID 43 Alopecia Areata 43 muscular dystrophy cystic fibrosis 43 genetic alterations 43 neuroinflammation 43 chronic lymphocytic leukemia 43 ocular albinism 43 telomere shortening 43 Hedgehog pathway 43 Brugada Syndrome 43 CFS ME 43 NKX2 43 thoracic aortic disease 43 cystic kidney 43 Beckwith Wiedemann Syndrome 43 aortic dissections 43 autoinflammatory diseases 43 ovarian tumors 43 Pervasive Developmental Disorder 43 PKD 43 Cystic Fibrosis CF 43 Fabry Disease 43 aortic dissection 43 bladder exstrophy 43 skeletal muscle weakness 43 SOD1 gene 43 Aplastic anemia 43 lupus nephritis 43 Acute myeloid leukemia 43 osteosarcoma bone 43 Tourette 43 Friedrich Ataxia 43 Alagille syndrome 43 Parkinsons Disease 43 systemic amyloidosis 43 lymphocytic leukemia 43 prosopagnosia 43 Fibrosis 43 astrocytomas 43 Relapsing Remitting MS 43 dominantly inherited 43 Dravet Syndrome 43 CMV infection 43 disease progression 43 autism spectrum 43 degenerative disease 43 MCADD 43 malignant brain 43 Sudden Unexplained Death 43 leukodystrophy 43 autism spectrum disorders ASDs 43 Autism 43 Coeliac disease 43 Leukemia 43 Stargardt disease 43 Myotonic dystrophy 43 incurable disease 43 recessive dystrophic epidermolysis bullosa 43 Ichthyosis 43 retinal detachment 43 alpha synuclein 43 cell acute lymphoblastic 43 pleural mesothelioma 43 polycystic kidney 43 developmental disorders 43 pancreatic cancer 43 progressive neurodegenerative disease 43 degenerative 43 #q#.# deletion syndrome 43 myocarditis 43 nonalcoholic cirrhosis 42 neurological disorder affecting 42 leukemias 42 sudden cardiac death 42 systemic lupus erythematosus SLE 42 degenerative neurological diseases 42 Prader Willi 42 Thalassemia 42 KIBRA 42 primitive neuroectodermal tumors 42 polymorphic ventricular tachycardia 42 Oxidative stress 42 myositis 42 presbycusis 42 autism neurological disorder 42 male pattern baldness 42 Aspergers Syndrome 42 neurobiological disorder 42 Inflammatory Bowel Disease 42 Tuberous Sclerosis 42 dyscalculia 42 degenerative disorders 42 Angelman 42 Parkinson's 42 chiari malformation 42 Prader Willi Syndrome 42 neurofibroma 42 MODY 42 chronic myelogenous leukemia 42 neurofibromas 42 acute lymphoblastic 42 rhabdomyosarcoma rare 42 teratoma 42 NOTCH1 42 chromosomal defects 42 respiratory syncytial virus 42 medulloblastoma malignant brain tumor 42 Cystic fibrosis 42 bone marrow stem cells 42 anterograde amnesia 42 polycystic ovarian syndrome PCOS 42 GBM tumors 42 savant syndrome 42 VHL 42 alveolar rhabdomyosarcoma 42 ceroid lipofuscinosis NCL 42 progressive neuromuscular 42 Aicardi Syndrome 42 myelodysplastic syndrome MDS 42 chronic kidney 42 idiopathic thrombocytopenic purpura 42 brainstem glioma 42 spinal muscle atrophy 42 congenital hypothyroidism 42 Premature Ovarian Failure 42 pulmonary fibrosis 42 Autism Spectrum Disorder 42 Graft Versus Host 42 TTTS 42 Shwachman Diamond Syndrome 42 deformed limbs 42 FMR1 gene 42 Li Fraumeni syndrome 42 disease epidermolysis bullosa 42 Beckwith Wiedemann syndrome 42 Wilms tumors 42 metastatic lung cancer 42 myelin breakdown 42 Parkinson Disease 42 PCNSL 42 Hypoplastic Left Heart 42 incurable degenerative disease 42 aspergers syndrome 42 Klotho gene 42 optic nerve hypoplasia 42 von Willebrand disease 42 CMV infections 42 relapsed AML 42 Hemochromatosis 42 acromegaly 42 nodular melanoma 42 metastatic cancer 42 scleroderma 42 CNVs 42 interstitial lung disease 42 Glioma 42 WT1 42 arthrogryposis 42 dimentia 42 paraganglioma 42 Neurofibromatosis type 42 congenital cataracts 42 Bardet Biedl syndrome 42 cranial radiation 42 chronic lymphocytic leukemia CLL 42 Vitamin B# deficiency 42 disease 42 RSV infection 42 autism Asperger 42 alopecia universalis 42 de novo mutations 42 choroidal melanoma 42 marrow transplant 42 Testicular cancer 42 Acute lymphoblastic leukemia 42 Asperger Syndrome AS 42 cortical dysplasia 42 premature menopause 42 HeFH 42 adrenoleukodystrophy 42 BRAF gene 42 progressive degeneration 42 tumor 42 diagnose Alzheimer disease 42 mutated protein 42 Acute Respiratory Failure 42 Klinefelter syndrome 42 lymphoma 42 Ewings sarcoma 42 Non Hodgkins Lymphoma 42 profound deafness 42 non hodgkins lymphoma 42 Tourette Syndrome 42 Dysplasia 42 Duchenne Becker 42 Morquio syndrome 42 EBV infection 42 Aileen Crowley 42 keratoconus 42 remyelination 42 Kate Sofia Vassilieva 42 Krabbe leukodystrophy 42 pheochromocytoma 42 Crigler Najjar syndrome 42 parainfluenza virus 42 CDH1 42 PTEN mutations 42 ALS amyotrophic lateral sclerosis 42 diabetes 42 medullary thyroid cancer 42 vasculitis 42 Hemophilia B 42 dystrophies 42 aortic aneurysms 42 fulminant hepatitis 42 Meckel Gruber 42 MYCN amplification 42 acute leukemias 42 CFTR gene 42 amyloid 42 GISTs 42 aneuploidy 42 McCune Albright 41 Alzheimers Disease 41 recurrent miscarriages 41 preeclampsia 41 verbal apraxia 41 chromosomal anomaly 41 Epstein Barr virus 41 ichthyosis 41 undiagnosed celiac disease 41 Ewings Sarcoma 41 fibrotic disease 41 lysosomal storage disease 41 lung metastasis 41 preventions treatments 41 cardiac channelopathies 41 leiomyosarcoma 41 alzheimer 41 atherosclerotic disease 41 ALS Amyotrophic Lateral Sclerosis 41 primordial dwarfism 41 tumor suppressor genes 41 degenerative nerve 41 hereditary degenerative 41 Bronchiectasis 41 Spinal muscular atrophy 41 clubfoot 41 Philadelphia Chromosome Positive 41 astrocytoma 41 inherited mutations 41 Crouzon syndrome 41 lateral sclerosis ALS 41 demyelinating disorders 41 de ath 41 Obsessive compulsive disorder 41 aortic valve stenosis 41 Thalassaemia 41 Fanconi Anaemia 41 Brittle Bone 41 growth hormone deficiency 41 spina bifida 41 Dravet 41 Wilm tumor 41 myelomeningocele 41 neurofibromatosis genetic disorder 41 hepatocellular carcinoma 41 inflammatory arthritis 41 neuropathies 41 acute myeloid 41 Essential Tremor 41 Kenadie 41 immuno deficiency 41 genetic neuromuscular disorder 41 Lou Gehrig disease 41 craniofacial 41 inoperable pancreatic cancer 41 Tourette Syndrome TS 41 xeroderma pigmentosum 41 progressive retinal degenerative 41 VUR 41 Asperger Syndrome 41 Juvenile Rheumatoid Arthritis 41 autism spectrum disorders ASD 41 VHL gene 41 nephritis 41 myeloproliferative neoplasms 41 glomerulonephritis 41 chronic myeloid leukemia CML 41 telomeres shorten 41 Tay Sachs Disease 41 Sjogren syndrome 41 ADHD 41 Cystic Fibrosis 41 carcinoid tumors 41 dermatomyositis 41 Ewing sarcoma bone 41 Alzheimer's 41 Friedreich Ataxia 41 ciliopathies 41 Carcinoid 41 infantile onset 41 microvascular angina 41 GIST tumors 41 Velculescu 41 celiac disease 41 DePinho 41 epilepsies 41 mitochondrial function 41 otosclerosis 41 eosinophilic disorders 41 onset Alzheimer disease 41 lung tumors 41 aortic rupture 41 1 diabetes T1D 41 premature ovarian 41 autistic spectrum 41 chromosomal instability 41 osteosarcomas 41 Essential tremor 41 autosomal dominant polycystic kidney 41 hippocampal dysfunction 41 retinopathy 41 nerve degeneration 41 CHARGE Syndrome 41 hedgehog signaling 41 hypothyroidism 41 nonhereditary 41 fronto temporal dementia 41 developmental abnormalities 41 bronchopulmonary dysplasia 41 synaptogenesis 41 hypereosinophilic syndrome 41 Battens Disease 41 GM1 gangliosidosis 41 Congenital Adrenal Hyperplasia 41 Autism Spectrum Disorders ASD 41 Cytomegalovirus 41 inherited degenerative 41 sCJD 41 systemic lupus 41 HIBM 41 Fatty Liver Disease 41 cerebral palsy 41 mental retardation epilepsy 41 Aplastic Anaemia 41 rheumatic disease 41 primary biliary cirrhosis 41 Ashwin Chitale 41 idiopathic epilepsy 41 autoimmune disorder 41 allogeneic bone marrow 41 Lennox Gastaut syndrome 41 spinal cord injury 41 Canavan Disease 41 clotting disorder 41 Lou Gherig Disease 41 variable immunodeficiency 41 heterotaxy 41 Leukaemia 41 shortened telomeres 41 Cushing Syndrome 41 1 Antitrypsin Deficiency 41 respiratory viral infections 41 Aortic stenosis 41 fibromatosis 41 WAGR syndrome 41 inoperable brain aneurysm 41 Apert Syndrome 41 Von Hippel Lindau 41 facioscapulohumeral muscular dystrophy 41 neurological dysfunction 41 maple syrup urine 41 genetic variations 41 Psoriasis 41 hemangioma 41 amyloid deposits 41 XMRV infection 41 Cerebral malaria 41 systemic scleroderma 41 familial pancreatic cancer 41 BRCA2 gene 41 acute leukemia AML 41 degenerative retinal diseases 41 diagnosing autism 41 disorder thalassemia 41 rare neurological disorder 41 debilitating neuromuscular 41 SOD1 41 Kleine Levin 41 gastrointestinal stromal tumor 41 nonautistic children 41 Cryptococcus neoformans 41 sensorineural hearing loss 41 thoracic aortic aneurysm 41 Treacher Collins 41 Tay Sachs 41 Sarcopenia 41 recessive mutations 41 podocytes 41 Tumour 41 myasthenia gravis MG 41 craniofacial abnormalities 41 Obsessive Compulsive Disorder OCD 41 Osteogenesis imperfecta 41 spontaneous remission 41 Parkinson disease neurodegenerative disorder 41 oligodendrogliomas 41 diaphragmatic hernia 41 chromosomal anomalies 41 Autoimmune disorders 41 inflammatory bowel disease 41 amyotrophic lateral sclerosis 41 HER2 positive breast cancer 41 liver cancer 41 onset Alzheimer 41 Arrhythmogenic Right Ventricular Cardiomyopathy 41 Glioblastoma multiforme GBM 41 Lesch Nyhan syndrome 41 amyloid plaque 41 Myocarditis 41 Meningioma 41 Polycystic kidney disease 41 Rhabdomyosarcoma rare 41 Autistic Disorder 41 Crohn disease 41 primary ciliary dyskinesia 41 desmoid tumor 41 vasculopathy 40 phenylketonuria 40 hormonal disorder 40 cystic fibrosis hereditary 40 CHDs 40 CD# mAb 40 AA amyloidosis 40 acute myelogenous 40 paraneoplastic 40 Arnold Chiari Malformation 40 Macular degeneration 40 neuro degenerative diseases 40 amyloid deposition 40 Iron deficiency anemia 40 Autism Spectrum Disorders 40 TLR3 40 MPS VI 40 retinitis pigmentosa degenerative 40 Retinitis Pigmentosa 40 Neurofibromatosis Type 40 multiple endocrine neoplasia 40 testicular cancers 40 Astrocytoma 40 HHV 6 40 quadriplegic cerebral palsy 40 LRRK2 gene 40 asperger syndrome 40 nephrotic syndrome 40 epigenetic changes 40 pancreatic tumor 40 pancreatic adenocarcinoma 40 myeloproliferative disorder 40 chromosomal abnormality 40 trichotillomania 40 degenerative neurological condition 40 JAK2 40 cleft lips cleft palates 40 ataxia telangiectasia AT 40 juvenile rheumatoid arthritis 40 Chronic Myeloid Leukemia 40 SSc 40 Mucopolysaccharidosis 40 neuroendocrine tumors 40 Peanut allergy 40 protein misfolding diseases 40 spontaneous mutations 40 Parkinson disease neurological disorder 40 haematological cancers 40 Tuberous Sclerosis Complex 40 inappropriate antidiuretic hormone SIADH 40 Ventricular Septal Defect