Related by context. All words. (Click for frequent words.) 77 Rett Syndrome 66 Angelman syndrome 66 Angelman Syndrome 65 mitochondrial disease 63 Friedreich ataxia 62 NF2 62 autism 62 epilepsy 61 mitochondrial dysfunction 61 congenital deafness 61 Fanconi anemia 61 chromosomal disorder 61 holoprosencephaly 61 myotonic dystrophy 61 Dravet syndrome 61 mitochondrial diseases 61 genetic disorder 61 Fragile X 60 neurodegenerative disorder 60 spinal muscular atrophy 60 Spinal Muscular Atrophy SMA 60 Spinal Muscular Atrophy 60 Fragile X syndrome 60 Duchenne Muscular Dystrophy DMD 60 biliary atresia 59 Duchenne muscular dystrophy 59 autism spectrum disorders 59 ataxia telangiectasia 59 NF1 59 neuroblastoma 59 progressive neurodegenerative disorder 59 chromosome abnormality 59 lupus 59 Leber congenital amaurosis 59 CHARGE syndrome 59 degenerative neurological disorder 59 neurofibromatosis 59 spinocerebellar ataxia 59 spinal muscular atrophy SMA 59 neuropsychiatric disorder 59 Duchenne muscular dystrophy DMD 58 neurodevelopmental disorder 58 muscular dystrophy 58 DiGeorge Syndrome 58 hereditary blindness 58 Progeria 58 dystrophy 58 Duchenne 58 medulloblastoma 58 retinal degeneration 58 Becker muscular dystrophy 58 Joubert syndrome 58 progeria 58 Niemann Pick disease 58 degenerative disorder 58 developmental disorders 58 inherited neurological disorder 58 Sanfilippo Syndrome 58 mitochondrial disorders 58 leukodystrophy 58 osteogenesis imperfecta 57 Muscular dystrophy 57 Alzheimers disease 57 Prader Willi syndrome 57 Lafora disease 57 Usher Syndrome 57 HGPS 57 lymphoblastic leukemia 57 brain malformation 57 ependymoma 57 Hurler syndrome 57 neurological disorder 57 Fragile X Syndrome 57 Alzheimer disease AD 57 Leber Congenital Amaurosis LCA 57 Duchenne Muscular Dystrophy 57 Rubinstein Taybi syndrome 57 autism neurological disorder 56 Batten Disease 56 juvenile myelomonocytic leukemia 56 ASDs 56 Pompe Disease 56 Aicardi Syndrome 56 juvenile diabetes 56 genetic defect 56 apraxia 56 cystinosis 56 Alzheimer disease 56 DIPG 56 infantile spasms 56 Noonan Syndrome 56 Neuroblastoma 56 Sanfilippo syndrome 56 hereditary disorder 56 neuromuscular disease 56 FSHD 56 neurodevelopment disorder 56 ectodermal dysplasia 56 developmental disorder 56 Krabbe Disease 56 retinoblastoma 56 MECP2 56 dyskeratosis congenita 56 neurodegenerative disease 56 autism spectrum disorder 56 polycystic kidney disease 56 Huntington Disease 56 neurodevelopmental disorders 56 leukemia ALL 56 DiGeorge syndrome 56 Rett syndrome neurological disorder 55 Chiari Malformation 55 Alport Syndrome 55 motor neuron disease 55 Tourette Syndrome TS 55 neuro developmental disorder 55 VCFS 55 Myasthenia gravis 55 metabolic disorder 55 MECP2 gene 55 fatal neuromuscular disorder 55 CdLS 55 Leber congenital amaurosis LCA 55 cystic fibrosis 55 autistic spectrum 55 blastoma 55 fronto temporal dementia 55 Mitochondrial Disease 55 Niemann Pick 55 chromosomal defect 55 inherited retinal degeneration 55 hereditary deafness 55 Cystic fibrosis 55 Fanconi Anaemia 55 neurological disorder affecting 55 Autism Spectrum Disorders 55 epidermolysis bullosa EB 55 Alzheimer 55 static encephalopathy 55 Krabbe disease 55 hypophosphatasia 55 congenital muscular dystrophy 55 incurable genetic 55 medulloblastomas 55 Wilms tumor 55 mitochondrial myopathy 54 rhabdomyosarcoma 54 Autism Spectrum Disorder ASD 54 limb girdle muscular dystrophy 54 Hutchinson Gilford progeria 54 FTLD 54 FSGS 54 Neurofibromatosis 54 motor neurone 54 dyscalculia 54 autistic 54 degenerative neurological disease 54 Parkinsons disease 54 achromatopsia 54 congenital adrenal hyperplasia CAH 54 Dravet Syndrome 54 neurobiological disorder 54 Adrenoleukodystrophy 54 gene MECP2 54 lysosomal storage diseases 54 MELAS 54 autoimmune disease 54 Cystic Fibrosis CF 54 ataxia 54 septo optic dysplasia 54 Leukodystrophy 54 Parkinson Disease 54 autosomal dominant 54 myasthenia gravis 54 autosomal dominant disorder 54 prion disease 54 Tuberous Sclerosis 54 tuberous sclerosis complex 54 Hydrocephalus 54 leukodystrophies 54 sporadic ALS 54 Aicardi syndrome 54 Fanconi Anemia 54 Myotonic dystrophy 53 Kufs disease 53 Diffuse Intrinsic Pontine Glioma 53 CHD7 53 Dystonia 53 Joubert Syndrome 53 NPHP 53 juvenile rheumatoid arthritis 53 polycystic ovary syndrome PCOS 53 Coeliac disease 53 Retinoblastoma 53 severe aplastic anemia 53 Cardiomyopathy 53 progressive neurological disorder 53 Polycystic kidney disease 53 FXTAS 53 inherited neurodegenerative disorder 53 Prader Willi Syndrome 53 Duchene muscular dystrophy 53 polycystic ovarian syndrome PCOS 53 genetic abnormality 53 Usher syndrome 53 Hurler Syndrome 53 neuro degenerative disorder 53 Angelman 53 epigenetic changes 53 epilepsies 53 MeCP2 gene 53 chronic granulomatous disease 53 verbal apraxia 53 cerebellar hypoplasia 53 spastic diplegia 53 Hutchinson Gilford Progeria Syndrome 53 PANDAS 53 neurodegeneration 53 G#S mutation 53 eosinophilic esophagitis 53 Six3 53 enzyme deficiency 53 Parkinsons Disease 53 Autism 53 JMML 53 Congenital Adrenal Hyperplasia 53 incurable neurological disorder 53 Battens Disease 53 Tuberous Sclerosis Complex 53 prosopagnosia 52 Alzheimers Disease 52 rheumatic disease 52 lymphoblastic lymphoma 52 alopecia areata 52 juvenile dermatomyositis 52 fatty liver disease 52 Alzheimer Disease 52 Pompe 52 autism spectrum disorders ASD 52 autism spectrum 52 Down syndrome 52 ADPKD 52 LHON 52 Niemann Pick Disease 52 Polycystic Kidney Disease 52 primary biliary cirrhosis 52 Proteus Syndrome 52 Canavan Disease 52 Asperger Disorder 52 fatal neurodegenerative disorder 52 autoimmunity 52 Ectodermal Dysplasia 52 sickle cell disease 52 CIDP 52 familial ALS 52 motor neuron diseases 52 pseudotumor cerebri 52 Cystinosis 52 Autism Spectrum Disorders ASD 52 Essential tremor 52 Cerebral palsy 52 Diamond Blackfan Anemia 52 Marfan syndrome 52 Pompe disease rare 52 embryonal rhabdomyosarcoma 52 biliary atresia rare 52 carcinoid cancer 52 genetic syndromes 52 MCAD deficiency 52 Leber Hereditary Optic Neuropathy 52 autoinflammatory diseases 52 Mitochondrial diseases 52 synovial sarcoma 52 Sandhoff disease 52 causative gene 52 dystonia 52 hepatoblastoma 52 acute myelogenous leukemia AML 52 obsessive compulsive disorder OCD 52 neuronal dysfunction 52 Medulloblastoma 52 Long QT Syndrome 52 Epilepsy 52 autism spectrum disorders ASDs 52 Hirschsprung disease 52 neurodevelopmental 52 rare neurological disorder 52 retinal degenerative disease 52 AAT deficiency 51 Lewy Body Dementia 51 Moebius Syndrome 51 facioscapulohumeral muscular dystrophy 51 neurofibromatosis type 51 adult neurogenesis 51 de novo mutations 51 beta thalassemia 51 autoimmune encephalitis 51 Severe Primary IGFD 51 Friedreich Ataxia 51 Endometriosis 51 chromosomal abnormality 51 Barth Syndrome 51 multiple sclerosis MS 51 Hutchinson Gilford Progeria 51 immunodeficiency disease 51 Ataxia 51 Alzhiemer 51 neuropsychiatric disorders 51 frontotemporal dementia 51 Cockayne syndrome 51 neuro degenerative disease 51 Pompe disease 51 FMR1 gene 51 Von Willebrand disease 51 LQTS 51 congenital hyperinsulinism 51 cerebal palsy 51 gene mutation 51 systemic lupus erythematosus SLE 51 Lupus 51 leukemia 51 schizophrenia 51 autosomal recessive 51 inherited neurodegenerative 51 dyslexia 51 Trisomy 51 chromosome abnormalities 51 primary immunodeficiency 51 degenerative disease 51 Marfan 51 lymphangioleiomyomatosis LAM 51 Leber Congenital Amaurosis 51 Aspergers Syndrome 51 Obsessive compulsive disorder 51 Pervasive Developmental Disorder 51 neurological dysfunction 51 inherited mutations 51 Peutz Jeghers syndrome 51 degenerative muscular 51 neuromuscular disorder 51 Friedrich Ataxia 51 clotting disorder 51 Tay Sachs disease 51 Inflammatory Breast Cancer 51 Li Fraumeni syndrome 51 Motor neurone disease 51 Pelizaeus Merzbacher disease 51 RSRF 51 huntingtin gene 51 Aspergers syndrome 51 fatal neurodegenerative 51 neurobehavioral disorder 51 degenerative neurological diseases 51 chromosome deletion 51 medium chain acyl 51 multisystem disorder 51 epidermolysis bullosa 51 immunodeficiencies 51 REM sleep behavior 51 Ataxia Telangiectasia 51 hypothalamic hamartoma 51 spontaneous mutations 51 retinitis pigmentosa RP 51 dyspraxia 51 mutated gene 50 protein tau 50 synaptic function 50 Beckwith Wiedemann Syndrome 50 immunodeficiency disorder 50 Downs Syndrome 50 atopic eczema 50 Pre eclampsia 50 optic atrophy 50 cognitive deficits 50 chromosomal anomaly 50 chiari malformation 50 Parkinson disease 50 Parkinson disease PD 50 Burkitt lymphoma 50 Leber hereditary optic neuropathy 50 Apert 50 GM1 gangliosidosis 50 hydrocephalus 50 cardiac hypertrophy 50 Stargardt disease 50 mitochondrial disorder 50 Alzheimers 50 Parkinsons 50 congenital disorder 50 Glioblastoma 50 autoimmune thyroiditis 50 Lennox Gastaut syndrome 50 Anencephaly 50 Porphyria 50 retinitis pigmentosa 50 Maroteaux Lamy syndrome 50 Acute Myelogenous Leukemia AML 50 Kawasaki Disease 50 Rotavirus infection 50 Cystic Fibrosis 50 muscular dystrophies 50 Macular degeneration 50 defective gene 50 Essential Tremor 50 familial hypercholesterolemia 50 Retinitis pigmentosa 50 retinal diseases 50 TTR amyloidosis 50 rare chromosomal disorder 50 Dyslexia 50 CNTNAP2 gene 50 von Willebrand disease 50 Chiari malformation 50 MPS VI 50 muscular dystrophy cystic fibrosis 50 pediatric brain tumor 50 Preeclampsia 50 preeclampsia 50 Osteogenesis Imperfecta 50 neuroblastomas 50 childhood disintegrative disorder 50 Fragile X. 50 CFS ME 50 Diamond Blackfan anemia 50 anorexia nervosa 50 craniosynostosis 50 compulsive hoarding 50 T1DM 50 kisspeptin 50 FMRP protein 50 achondroplasia 50 developmental disability 50 myasthenia gravis MG 50 hereditary degenerative 50 Dravet 50 progressive neurodegenerative 50 profound deafness 50 medulloblastoma tumors 50 disabling neurological 50 onset Alzheimer disease 50 Chronic fatigue 50 CALHM1 50 Rhabdomyosarcoma 50 Krabbe Leukodystrophy 50 hemophagocytic lymphohistiocytosis 50 optic nerve hypoplasia 50 progressive neurodegenerative disease 50 Tourette 50 autism Asperger 50 systemic scleroderma 50 Progeria Research 50 iron overload 50 JAK mutations 50 generalized epilepsy 50 Fanconi anemia rare 50 Marfan Syndrome 50 Osteosarcoma 50 Childhood Disorder 50 Aplastic anemia 50 Cockayne Syndrome 50 Apert syndrome 50 Alzheimer Disease AD 50 onset Alzheimer 50 Langerhans Cell Histiocytosis 50 neuro muscular disorder 50 PIDD 50 Reactive Attachment Disorder 50 Aplastic Anemia 50 polycystic ovary syndrome 49 dysautonomia 49 Scleroderma 49 congenital diaphragmatic hernia 49 petit mal seizures 49 neuronal degeneration 49 dominantly inherited 49 acute myeloid leukemia 49 excitotoxicity 49 Nephrotic Syndrome 49 ADHD 49 progeria rare 49 hereditary spastic paraplegia 49 Tay Sachs Disease 49 spinocerebellar ataxia type 49 disorder ASD 49 disorder thalassemia 49 Tourette syndrome 49 alpha synuclein gene 49 cerebellar ataxia 49 Prader Willi 49 Hashimoto thyroiditis 49 Ewing sarcoma 49 multiple sclerosis 49 herpes viruses 49 cystic fibrosis CF 49 Wilms Tumor 49 autistic tendencies 49 Autism Spectrum Disorder 49 acute lymphocytic leukemia 49 #q#.# deletion syndrome 49 susceptibility gene 49 Brugada Syndrome 49 neuronal function 49 Meckel Gruber 49 precocious puberty 49 auditory neuropathy 49 IL#R 49 histiocytosis 49 tuberous sclerosis 49 epigenetic alterations 49 debilitating neurological disorder 49 HLH 49 incurable neurodegenerative disease 49 epileptic seizures 49 Spinal muscular atrophy 49 vulvodynia 49 Acute Myelogenous Leukemia 49 Wilm Tumor 49 Myositis 49 KIBRA 49 1 Antitrypsin Deficiency 49 narcolepsy cataplexy 49 RPE# 49 ARVD 49 galactosemia 49 neurogenetic 49 Polycystic Ovary Syndrome 49 Asberger syndrome 49 neuroblastoma tumor 49 intractable epilepsy 49 nephrotic syndrome 49 hereditary breast cancer 49 polyglutamine diseases 49 nonsense mutation 49 retinal dysfunction 49 ependymomas 49 amyloidosis 49 hemiplegia 49 motor neuron degeneration 49 Parkinson degenerative 49 Frontotemporal Dementia 49 primitive neuroectodermal tumors 49 ataxias 49 cortical dysplasia 49 Apraxia 49 Asberger Syndrome 49 Acute lymphocytic leukemia 49 WAGR syndrome 49 dysregulated 49 incurable hereditary 49 Autistic Spectrum Disorders 49 MODY 49 kernicterus 49 chronic autoimmune disorder 49 cerebral palsy 49 neurofibrillary 49 neurodegenerative disorders 49 Klinefelter syndrome 49 allergic asthma 49 idiopathic epilepsy 49 demyelination 49 Retinitis Pigmentosa RP 49 Postpartum depression 49 Wiskott Aldrich syndrome 49 multisystem disease 49 cerebral palsy epilepsy 49 myelomeningocele 49 autosomal recessive genetic 49 prion diseases 49 neurodegenerative diseases 49 dilated cardiomyopathy 49 myotonia 49 myotonic muscular dystrophy 49 developmentally delayed 49 TTTS 49 neurobehavioral disorders 49 Autistic Disorder 49 lissencephaly 49 type 1diabetes 49 Langerhans cell histiocytosis 49 cytomegalovirus CMV 49 autistic regression 49 pre eclampsia 49 disease NAFLD 48 genetic neuromuscular disorder 48 transgenic mouse models 48 myelodysplasia 48 Stargardt Disease 48 involuntary tics 48 PKU genetic 48 degenerative neurological condition 48 xeroderma pigmentosum 48 neurofibromatosis NF 48 Beckwith Wiedemann syndrome 48 congenital blindness 48 Gestational diabetes 48 dementia 48 complex neurobiological disorder 48 developmental abnormalities 48 recessively inherited 48 celiac disease 48 juvenile myoclonic epilepsy 48 monogenic 48 amyloid cascade 48 essential thrombocythemia 48 asperger syndrome 48 aplastic anemia 48 protein misfolding 48 Hemochromatosis 48 Trichotillomania 48 myeloproliferative neoplasms 48 diffuse intrinsic pontine glioma 48 Asperger Syndrome AS 48 dyslexia dyspraxia 48 Cowden syndrome 48 Myelodysplastic syndrome 48 Wiskott Aldrich Syndrome 48 preventions treatments 48 amyotrophic lateral sclerosis ALS 48 metachromatic leukodystrophy 48 Cushing syndrome 48 Amyotrophic lateral sclerosis ALS 48 Schizophrenia 48 Lou Gherig disease 48 genetic mutation 48 CNTNAP2 48 Premature Ovarian Failure 48 Morquio Syndrome 48 alzheimer 48 progressive degeneration 48 alzheimer disease 48 protein misfolding diseases 48 paraneoplastic 48 Parkinson sufferers 48 neuropathology 48 gastrointestinal dysfunction 48 Duchene Muscular Dystrophy 48 Autistic Spectrum Disorder 48 mild cognitive 48 Parkinson disease neurodegenerative disorder 48 progressive degenerative neurological 48 chromosomal anomalies 48 neuroendocrine 48 Major depressive disorder 48 galanin 48 otosclerosis 48 blood clotting disorder 48 behavioral disinhibition 48 familial adenomatous polyposis 48 HbF 48 Acute Lymphoblastic Leukemia 48 lysosomal storage disease 48 acute lymphatic leukemia 48 Stargardt Macular Dystrophy 48 Proteus syndrome 48 mental retardation epilepsy 48 mutant genes 48 spinal muscle atrophy 48 Wilms Tumour 48 bronchopulmonary dysplasia 48 ocular albinism 48 hypothyroidism 48 hydrops 48 renal fibrosis 48 T2D 48 Wnt signaling pathway 48 deafness 48 tau pathology 48 T1D 48 hyperemesis 48 Iron deficiency anemia 48 nerve degeneration 48 AAT Deficiency 48 autosomal dominant polycystic kidney 48 SOD1 48 lysosomal diseases 48 postpartum depression PPD 48 genetic disorders 48 Congenital Muscular Dystrophy 48 fungal meningitis 48 autistics 48 dystonia neurological movement 48 immunodeficiency 48 Amyotrophic Lateral Sclerosis ALS 48 Juvenile Diabetes 48 Cholangiocarcinoma 48 Keratoconus 48 syringomyelia 48 neuropsychiatric diseases 48 protein dystrophin 48 scoliosis 48 carcinoid 48 Polycystic Ovarian Syndrome PCOS 48 Parkinson's 48 variable immunodeficiency 48 Neurofibromatosis Type 48 Down syndrome chromosomal disorder 48 Spina Bifida 48 mosaicism 48 pneumococcal meningitis 48 progranulin mutations 48 Rhabdomyosarcoma rare 48 hypertrophic cardiomyopathy HCM 48 DiGeorge syndrome rare 48 DISC1 gene 48 Atopic dermatitis 48 Ewing Sarcoma 48 Celiac disease 48 Fanconi 48 Retinopathy 48 alpha synuclein 48 Hirschsprung Disease 48 neurodevelopmental disability 48 breast cancer metastasis 48 chronic fatigue syndrome 48 pigmentosa 48 Austism 48 Tay Sachs 48 mastocytosis 48 Brittle Bone 48 restrictive cardiomyopathy 48 Premature ejaculation 48 trichotillomania 48 Multiple Sclerosis 48 hypereosinophilic syndrome 48 Stargardt 48 Cystic fibrosis CF 48 Sjögren syndrome 48 Kleine Levin 48 Interstitial cystitis 48 Myelin Project 48 Ehlers Danlos syndrome 48 Sudden Unexplained Death 48 Peanut allergy 48 Epstein Barr Virus 48 Macular Degeneration 48 diffuse pontine glioma 48 LRRK2 gene 48 Dyspraxia 48 neurofibromas 48 SMN protein 48 hormonal disorder 48 quadriplegic cerebral palsy 47 skeletal dysplasia 47 Biliary Atresia 47 fibrodysplasia ossificans progressiva FOP 47 Restless Legs Syndrome 47 malignant transformation 47 interferon pathway 47 chorea 47 GIST tumors 47 metabolic abnormalities 47 Brugada syndrome 47 basal cell nevus syndrome 47 wet macular degeneration 47 Alzheimer pathology 47 IRAK1 47 prematurity ROP 47 cognitive dysfunction 47 developmental delays 47 synaptogenesis 47 dissociative disorders 47 gastric carcinoma 47 mental retardation 47 congenital disorders 47 aphasia 47 aneuploidies 47 Beta thalassemia 47 astrocytomas 47 ventricular dysplasia 47 Parkinson disease degenerative 47 genetic abnormalities 47 postpartum mood 47 EoE 47 Glioma 47 HIBM 47 choriocarcinoma 47 brain lesions 47 polycystic disease 47 Attention Deficit Hyperactive Disorder 47 behavioral abnormalities 47 thyroiditis 47 scleroderma 47 acute lymphoid leukemia 47 MYH9 gene 47 Meckel Gruber syndrome 47 Juvenile Arthritis 47 Cerebral malaria 47 Rh incompatibility 47 mutant protein 47 IL 7R 47 Obstructive sleep apnea 47 euthymic patients 47 Spina bifida 47 Menkes disease 47 hemolytic anemia 47 Asperger 47 myelination 47 IDH1 47 Mild cognitive impairment 47 acute promyelocytic leukemia 47 Fatty liver 47 Moyamoya disease 47 inherited metabolic disorders 47 cystic fibrosis hereditary 47 Cryptococcus neoformans 47 myelogenous leukemia 47 herpesviruses 47 lung fibrosis 47 Familial Dysautonomia 47 CMV infection 47 debilitating autoimmune 47 maternally inherited 47 DBMD 47 disease 47 neurological abnormalities 47 Autoimmune disorders 47 Endometrial cancer 47 sensorineural hearing loss 47 atypical hemolytic uremic syndrome 47 microdeletion 47 mitochondrial function 47 mutated genes 47 MYCN amplification 47 ATTR 47 alpha thalassemia 47 amyloid toxicity 47 SHANK3 47 spastic cerebral palsy 47 Autoimmune diseases 47 arthrogryposis 47 Hemophilia B 47 dysbindin 47 Sudden Arrhythmia Death 47 autosomal recessive disorder 47 Down Syndrome 47 leukoencephalopathy 47 Hereditary angioedema HAE 47 autism cerebral palsy 47 Polycystic Ovary Syndrome PCOS 47 chromosomal abnormalities 47 hereditary disorders 47 transdifferentiation 47 occipital regions 47 neurological 47 PGRN 47 Wernicke Korsakoff syndrome 47 chromosomal imbalance 47 ciliopathies 47 muscle degeneration 47 Shwachman Diamond Syndrome 47 urological cancers 47 systemic lupus 47 myositis 47 brainstem glioma 47 Huntington Chorea 47 SHANK3 gene 47 FMR1 47 IKK2 47 interstitial cystitis 47 congenital hypothyroidism 47 spasmodic dysphonia 47 pulmonary hypertension 47 autoimmune disorder 47 pyloric stenosis 47 Aortic stenosis 47 autistic traits 47 PKD 47 X SCID 47 ASD 47 idiopathic generalized epilepsy 47 Eosinophilic 47 recurrent infections 47 microchimerism 47 hematologic disorders 47 spastic paraplegia 47 apoE4 47 neuroinflammation 47 tics involuntary 47 Narcolepsy 47 HELLP 47 Burkitt Lymphoma 47 dermatomyositis 47 porphyria 47 medulloblastoma malignant brain tumor 47 ichthyosis 47 degenerative nerve disorder 47 behavioral disturbances 47 ALS 47 pathogenic mechanisms 47 Spinal cord injury 47 juvenile idiopathic arthritis 47 HHV 6 47 truncus arteriosus 47 Alzheimer disease pathology 47 temporal lobe epilepsy 47 hematological abnormalities 47 chordoma 47 synaesthesia 47 neurological impairments 47 jerky involuntary 47 Oppositional Defiant Disorder 47 RDEB 47 lymphocytic leukemia 47 filaggrin 47 Beta Thalassemia 47 diabetes mellitus DM 47 Acute Lymphoblastic Leukaemia 47 leukemia AML 47 androgenetic alopecia 47 leukaemias 47 nonalcoholic cirrhosis 47 selective mutism 47 Myocarditis 47 dementing 47 mitochondrial mutations 47 Wolf Hirschhorn 47 Klotho gene 47 alveolar rhabdomyosarcoma 47 untreated celiac disease 47 Ets2 47 debilitating neurological disease 47 acute lymphoblastic leukemia 47 progressive retinal degenerative 47 STAT4 47 Phenylketonuria PKU 46 Inflammatory Bowel 46 juvenile idiopathic arthritis JIA 46 cardiomyopathy 46 IgA deficiency 46 Chronic Myeloid Leukemia 46 cystic kidney 46 SOD1 gene 46 FRAXA 46 underlying pathophysiology 46 phenylketonuria 46 CFTR gene 46 neurodegenerative 46 Glioblastoma Multiforme GBM 46 CHARGE Syndrome 46 homozygous FH 46 myeloproliferative disorders 46 Juvenile Idiopathic Arthritis JIA 46 ApoE gene 46 Polycystic ovary syndrome PCOS 46 Velculescu 46 tic disorders 46 airway hyperresponsiveness 46 disorder FASD 46 neural tube defect 46 Hodgkin Lymphoma 46 attention-deficit/hyperactivity disorder ADHD 46 bipolar illness 46 premature ovarian 46 microcephaly 46 neurological disorders 46 mood disorders 46 uncontrolled epilepsy 46 aneuploidy 46 mutant gene 46 hereditary hemochromatosis 46 Von Hippel Lindau 46 Hereditary angioedema 46 recurrent miscarriages 46 cognitive impairments 46 Syringomyelia 46 Alport syndrome 46 hyperactivation 46 cerebral palsy Down syndrome 46 proliferative diabetic retinopathy 46 cystic fibrosis Duchenne muscular 46 APOE4 46 involuntary movements 46 transverse myelitis 46 vitamin B# deficiency 46 irreversible blindness 46 IUGR 46 Savant Syndrome 46 leptin resistance 46 FASPS 46 subclinical hypothyroidism 46 gene p# 46 Wilm tumor 46 Aspergers 46 CHDs 46 degenerative neuromuscular disease 46 Dysautonomia 46 EBV infection 46 Severe Combined Immunodeficiency 46 leukemia lymphoma myeloma 46 Acute Lymphocytic Leukemia 46 myeloproliferative diseases 46 endometriosis 46 C1q 46 Asperger syndrome milder 46 Fetal Alcohol Syndrome 46 demyelinating disorders 46 neurofibroma 46 idiopathic pulmonary fibrosis IPF 46 generalized seizures