Related by context. All words. (Click for frequent words.) 67 Fragile X Syndrome 66 Fragile X 62 genetic disorder 61 mitochondrial dysfunction 60 genetic defect 60 Rett syndrome 60 developmental disorder 59 chromosome abnormality 59 autism spectrum disorders 58 FXTAS 58 Angelman syndrome 58 degenerative disorder 58 spinal muscular atrophy SMA 58 hereditary disorder 58 NF2 58 neuropsychiatric disorder 58 autosomal recessive 58 Fanconi anemia 58 mitochondrial disorders 58 myotonic dystrophy 57 FMR1 gene 57 ASDs 57 Fragile X. 57 Friedreich ataxia 57 autism spectrum disorder 57 Angelman Syndrome 57 gene mutation 57 neurodevelopmental disorder 57 Duchenne muscular dystrophy 57 autism 57 neurobiological disorder 57 Dravet syndrome 57 neurodegenerative disorder 57 Niemann Pick disease 56 Leber congenital amaurosis 56 Rubinstein Taybi syndrome 56 chromosomal defect 56 mitochondrial disease 56 congenital deafness 56 Leber congenital amaurosis LCA 56 mutated gene 56 neurodegenerative disease 56 FTLD 55 REM sleep behavior 55 autism spectrum disorders ASDs 55 metabolic disorder 55 NF1 55 Tourette syndrome 55 eosinophilic esophagitis 55 neurological disorder 55 neurodevelopmental disorders 55 Tay Sachs disease 55 neurofibromatosis 55 familial adenomatous polyposis 55 defective gene 55 narcolepsy cataplexy 55 ataxia telangiectasia 55 Hutchinson Gilford progeria 55 inherited neurological disorder 55 APOE4 55 Asperger Disorder 54 autosomal dominant 54 enzyme deficiency 54 genetic abnormality 54 chromosomal disorder 54 ADHD 54 susceptibility gene 54 Obstructive sleep apnea 54 Duchenne muscular dystrophy DMD 54 incurable neurological disorder 54 developmental disorders 54 progressive neurodegenerative disorder 54 genetic mutation 54 CNTNAP2 54 Sanfilippo Syndrome 54 Spinal Muscular Atrophy 54 Lafora disease 54 Polycystic kidney disease 54 G#S mutation 54 Duchenne 54 cardiac hypertrophy 54 Alport syndrome 54 protein misfolding 54 neuropsychiatric disorders 54 dyscalculia 54 mitochondrial diseases 54 neuro developmental disorder 54 fatty liver disease 53 Hurler syndrome 53 osteogenesis imperfecta 53 Noonan Syndrome 53 protein tau 53 LQTS 53 CHARGE syndrome 53 autism spectrum 53 cystic fibrosis 53 Marfan syndrome 53 neuroblastoma 53 attention-deficit/hyperactivity disorder 53 genetic disorders 53 leukemia ALL 53 HGPS 53 juvenile idiopathic arthritis 53 Hyperactivity Disorder 53 MECP2 gene 53 Muscular dystrophy 53 CNTNAP2 gene 53 retinoblastoma 53 AAT deficiency 53 Leber Hereditary Optic Neuropathy 53 fatal neurodegenerative disorder 53 Fragile X gene 53 fatal neurodegenerative 53 Medulloblastoma 53 Hashimoto thyroiditis 53 Down syndrome chromosomal disorder 53 juvenile idiopathic arthritis JIA 53 Alzheimers disease 53 neurological disorder affecting 53 inherited mutations 53 CHD7 53 WAGR syndrome 53 Hutchinson Gilford Progeria Syndrome 53 Pelizaeus Merzbacher disease 53 medulloblastoma 53 attention-deficit/hyperactivity disorder ADHD 53 Alzheimer disease AD 53 hypophosphatasia 53 Alport Syndrome 53 Cystic fibrosis 53 epilepsy 53 apraxia 53 holoprosencephaly 53 auditory neuropathy 53 neurobehavioral disorder 53 FMRP protein 53 medulloblastomas 52 inherited retinal degeneration 52 dyskeratosis congenita 52 familial hypercholesterolemia 52 spinal muscle atrophy 52 autism neurological disorder 52 Asperger syndrome milder 52 lysosomal storage diseases 52 seizure disorders 52 pseudotumor cerebri 52 infantile spasms 52 Myotonic dystrophy 52 phenylketonuria 52 Meckel Gruber 52 sporadic ALS 52 Duchenne Muscular Dystrophy 52 ectodermal dysplasia 52 Pompe Disease 52 Tourette syndrome neurological disorder 52 lysosomal storage disease 52 disorder ADHD 52 CNVs 52 Progeria 52 Cockayne Syndrome 52 MODY 52 DiGeorge syndrome 52 Von Willebrand disease 52 von Willebrand disease 52 neurofibromatosis type 52 familial ALS 52 synaptic plasticity 52 epigenetic changes 52 Kufs disease 52 degenerative neurological diseases 52 genetically inherited 52 WDR# 52 JAK mutations 52 Alzheimer Disease AD 52 autism spectrum disorders ASD 52 gene MECP2 52 progressive neurodegenerative disease 52 MCAD deficiency 52 developmental disability 52 genetic variant 52 Rett Syndrome 51 inflammatory bowel disease 51 Obsessive compulsive disorder 51 neurodevelopmental 51 Stargardt disease 51 chronic granulomatous disease 51 MELAS 51 primary biliary cirrhosis 51 Major depressive disorder 51 myasthenia gravis 51 #q#.# [001] 51 genetic mutations 51 Autoimmune disorders 51 mutant gene 51 degenerative neurological disorder 51 Severe Combined Immunodeficiency 51 ADPKD 51 Prader Willi syndrome 51 Maroteaux Lamy Syndrome 51 Usher syndrome 51 neuroblastomas 51 T1DM 51 Cockayne syndrome 51 Leber Congenital Amaurosis LCA 51 achromatopsia 51 Hemophilia B 51 Brugada Syndrome 51 LRRK2 51 juvenile myelomonocytic leukemia 51 Krabbe disease 51 disorder ASD 51 FSGS 51 FASPS 51 Autism Spectrum Disorders 51 Usher Syndrome 51 mutated genes 51 disorders 51 spinocerebellar ataxia 51 dyspraxia 51 tuberous sclerosis complex 51 mitochondrial myopathy 51 Peanut allergy 51 LIS1 51 progeria 51 RPE# 51 Retinoblastoma 51 gene variant 51 Essential tremor 51 Wiskott Aldrich syndrome 51 Krabbe Leukodystrophy 51 insulin resistance 51 behavioral abnormalities 51 FSHD 51 ataxias 51 Coeliac disease 51 Sanfilippo syndrome 51 medium chain acyl 51 Irritable bowel syndrome IBS 51 chromosomal translocations 51 juvenile rheumatoid arthritis 51 hereditary deafness 51 optic nerve hypoplasia 51 Retinitis pigmentosa 51 chronic autoimmune disorder 51 Cerebral palsy 51 sickle cell disease 51 Duchenne Muscular Dystrophy DMD 51 Li Fraumeni syndrome 51 brain malformation 51 Severe Primary IGFD 50 dysbindin gene 50 acute myelogenous leukemia AML 50 schizophrenia 50 Hutchinson Gilford Progeria 50 apoE4 50 Childhood Disorder 50 Becker muscular dystrophy 50 neurologic disorders 50 Pervasive Developmental Disorder 50 tuberous sclerosis 50 JMML 50 spastic diplegia 50 skeletal dysplasia 50 vWD 50 epigenetic alterations 50 CdLS 50 Tuberous Sclerosis Complex 50 de novo mutations 50 neuromuscular disease 50 HeFH 50 systemic lupus erythematosus SLE 50 Joubert syndromes 50 Retinopathy 50 mutation 50 fatal neuromuscular disorder 50 Mitochondrial diseases 50 PKU genetic 50 genetic abnormalities 50 Asperger disorder 50 ependymoma 50 disorders ASD 50 verbal apraxia 50 neurological 50 developmental delays 50 neurodegeneration 50 hemochromatosis 50 homozygous FH 50 ADHD Attention Deficit 50 anaplastic lymphoma kinase 50 acute leukemias 50 neurological disorders 50 retinal degeneration 50 synaptogenesis 50 Gaucher disease 50 mitochondrial mutations 50 CFTR gene 50 mtDNA mutations 50 rheumatic disease 50 EoE 50 motor neuron diseases 50 MPS VI 50 myelodysplasia 50 leukodystrophies 50 autism Asperger 50 neurofibromatosis genetic disorder 50 Lesch Nyhan syndrome 50 frontotemporal dementia 50 huntingtin gene 50 Celiac disease 50 Tourette Syndrome TS 50 ataxia 50 neurodevelopment disorder 50 HNPCC 50 mosaicism 50 homozygous familial hypercholesterolemia 50 Treacher Collins syndrome 50 Wilms tumor 50 Autism Spectrum Disorder 50 spinocerebellar ataxia type 50 leptin resistance 50 Crigler Najjar syndrome 50 APOE 50 Marfan Syndrome 50 Lennox Gastaut syndrome 50 juvenile myoclonic epilepsy 50 VUR 50 AAT Deficiency 50 recessive genetic 50 autoinflammatory diseases 50 Attention Deficit Hyperactive Disorder 50 atopic eczema 50 juvenile diabetes 50 retinal degenerative disease 50 synaptic function 50 amblyopia 50 Rett syndrome neurological disorder 50 Atopic dermatitis 50 MYCN amplification 50 inherited predisposition 49 autosomal recessive disease 49 Vitamin D insufficiency 49 Aspergers syndrome 49 susceptibility genes 49 Down syndrome 49 obsessive compulsive disorder OCD 49 cystic fibrosis CF 49 genetic defects 49 nonsense mutations 49 Parkinson disease degenerative 49 DLX5 49 chromosomal anomaly 49 cognitive deficits 49 muscular dystrophy 49 signaling molecule 49 Vitamin B# deficiency 49 myeloproliferative neoplasms 49 nonsense mutation 49 congenital adrenal hyperplasia CAH 49 Krabbe Disease 49 Restless Legs Syndrome 49 psychiatric disorders 49 muscular dystrophies 49 dominantly inherited 49 persistent pulmonary hypertension 49 nephrotic syndrome 49 Niemann Pick 49 mastocytosis 49 Joubert syndrome 49 sleep disordered breathing 49 chromosomal abnormality 49 Spinal muscular atrophy 49 Peutz Jeghers syndrome 49 Long QT syndrome 49 hypertrophic cardiomyopathy HCM 49 ADAM# 49 pyloric stenosis 49 inherited metabolic disorders 49 tic disorders 49 recessive gene 49 Klinefelter syndrome 49 lymphoblastic leukemia 49 Bardet Biedl syndrome 49 genetic determinants 49 immunodeficiency disorder 49 genetic variations 49 VCFS 49 neurodegenerative disorders 49 neurological diseases 49 dwarfism 49 prosopagnosia 49 genetic syndromes 49 congenital blindness 49 FMR1 49 mutant protein 49 developmental abnormalities 49 dopamine receptor gene 49 hereditary predisposition 49 chronic neurological disorder 49 Fanconi Anemia 49 autoimmune disease 49 Hemochromatosis 49 polycystic kidney disease 49 immunodeficiency 49 KIBRA 49 Aspergers Syndrome 49 inflammatory bowel diseases 49 neurologic disorder 49 alopecia areata 49 Stargardt Macular Dystrophy 49 basal cell nevus syndrome 49 PTPN# 49 CALHM1 49 Osteosarcoma 49 biochemical imbalance 49 associated tremor ataxia 49 mutations 49 invasive secretory carcinoma 49 hydrops 49 autoimmune 49 childhood disintegrative disorder 49 Leber hereditary optic neuropathy 49 retinitis pigmentosa 49 neuronal dysfunction 49 muscular dystrophy cystic fibrosis 49 limb girdle muscular dystrophy 49 immunodeficiencies 49 neurodevelopment 49 Excessive daytime sleepiness 49 euthymic patients 49 onset diabetes 49 epilepsies 49 filaggrin 49 PDD NOS 49 optic neuropathy NAION 49 APOE e4 49 disorder 49 fatal myelination disorder 49 microcephalin 49 DISC1 49 degenerative neurological disease 49 selective mutism 49 dystrophy 49 Hypertrophic cardiomyopathy 49 carcinoid cancer 48 Spinal Muscular Atrophy SMA 48 Parkinsons disease 48 synapse formation 48 mGluR5 antagonist 48 recessive mutations 48 DISC1 gene 48 recessively inherited 48 LRRK2 gene 48 inherited neurodegenerative disorder 48 progressive neurological disorder 48 acute lymphoblastic 48 neurodevelopmental disorder characterized 48 polycystic ovary syndrome PCOS 48 ApoE gene 48 Juvenile Idiopathic Arthritis JIA 48 VHL gene 48 Autistic Disorder 48 Tourette Syndrome neurological disorder 48 APOE gene 48 disease NAFLD 48 LRAT 48 neurogenetic 48 facioscapulohumeral muscular dystrophy 48 hypocretin 48 cognitive dysfunction 48 autosomal dominant disorder 48 gastrointestinal dysfunction 48 lymphangioleiomyomatosis LAM 48 phthalate syndrome 48 intractable epilepsy 48 Premature birth 48 apoE 48 hereditary hemochromatosis 48 Parkinson degenerative 48 Pervasive Developmental Disorders 48 recessive trait 48 precocious puberty 48 neuro degenerative disease 48 obstructive sleep apnea 48 lissencephaly 48 Long QT Syndrome 48 acute promyelocytic leukemia 48 manic depressive disorder 48 celiac sprue 48 Bed wetting 48 genetic susceptibility 48 idiopathic thrombocytopenic purpura 48 Duchene muscular dystrophy 48 malignant transformation 48 Hirschsprung disease 48 Pompe disease 48 prion disease 48 neurodegenerative 48 RLS 48 familial pancreatic cancer 48 iron deficiency 48 IGFBP2 48 polycystic ovary syndrome 48 thyroiditis 48 plasma kallikrein 48 Periodontal disease 48 p# gene 48 neurodegenerative diseases 48 metabolic abnormalities 48 nerve degeneration 48 rhabdomyosarcoma 48 galactosemia 48 paraneoplastic 48 cystinosis 48 IDH1 48 irreversible blindness 48 savant syndrome 48 DiGeorge Syndrome 48 X chromosome 48 Iron deficiency anemia 48 neurofibrillary tangles 48 Myasthenia gravis 48 SHANK3 gene 48 onset Alzheimer disease 48 hyperprolactinemia 48 spontaneous mutations 48 Glioblastoma 48 neurobehavioral disorders 48 neural circuitry 48 Philadelphia Chromosome Positive 48 epigenetic 48 autistic traits 48 intestinal inflammation 48 SORL1 48 cystic fibrosis Duchenne muscular 48 serotonin defects 48 gene mutations 48 serotonin receptor 48 Attention Deficit Hyperactivity Disorder 48 IL#R 48 Lennox Gastaut Syndrome 48 neuroligins 48 blastoma 48 leukaemias 48 IgA deficiency 48 mental retardation syndromes 48 psychosocial dwarfism 48 ceroid lipofuscinosis NCL 48 common disabling neurological 48 underlying pathophysiology 48 Acute lymphoblastic leukemia 48 variable immunodeficiency 48 Wiskott Aldrich Syndrome 48 spinal muscular atrophy 48 Six3 48 ARVD 48 polymyalgia rheumatica 48 androgenetic alopecia 48 unprovoked seizures 48 tics involuntary 48 Tourette syndrome TS 48 amyotrophic lateral sclerosis ALS 48 mild cognitive 48 celiac disease 48 Oppositional Defiant Disorder 48 TACI 48 ADHD symptoms 48 EBV infection 48 Neurofibromatosis type 48 Leber Congenital Amaurosis 48 MIF gene 48 ApoE4 48 autoinflammatory 48 PTEN mutations 48 Proteus syndrome 48 Autism Spectrum Disorder ASD 48 pediatric bipolar disorder 48 tau pathology 48 Testicular cancer 48 Restless legs 48 sleep disorder narcolepsy 48 syndrome RLS 47 GM1 gangliosidosis 47 birth defect 47 autistic tendencies 47 chromosome deletion 47 Allergic rhinitis 47 Diffuse Intrinsic Pontine Glioma 47 molecular pathway 47 Chronic insomnia 47 Macular degeneration 47 carcinoid syndrome 47 dysregulation 47 neuronal plasticity 47 Thrombocytopenia 47 dopamine signaling 47 progressive neurodegenerative 47 LHON 47 Wnt signaling pathway 47 chromosome #q#.# [001] 47 systemic lupus erythematosus 47 Gynecomastia 47 ambiguous genitalia 47 primary pulmonary hypertension 47 hereditary spastic paraplegia 47 MECP2 47 Celiac sprue 47 immunodeficiency disease 47 DQB1 * 47 #q# deletion 47 G6PD deficiency 47 COMT gene 47 neural tube defect 47 Retinitis Pigmentosa RP 47 pulmonary hypertension PH 47 autistic spectrum 47 Smith Lemli Opitz 47 achondroplasia 47 non syndromic 47 neurobiological disorders 47 gluten intolerance 47 epigenetic silencing 47 myasthenia gravis MG 47 abnormal hemoglobin 47 allergic asthma 47 Primary IGFD 47 dysregulated 47 Iron deficiency 47 metabolic abnormality 47 Tay Sachs thalassemia 47 untreated sleep apnea 47 Klinefelter Syndrome 47 macular edema 47 Chronic fatigue 47 Irritable Bowel Syndrome 47 Neuroblastoma 47 presbycusis 47 GPC5 47 aciduria 47 SMN protein 47 Beta thalassemia 47 psoriasis psoriatic arthritis 47 PANDAS 47 Asberger Syndrome 47 myelogenous leukemia 47 #q#.# deletion syndrome 47 ApoE4 gene 47 sexsomnia 47 syndrome FAS 47 Parkinson disease neurodegenerative disorder 47 gene variation 47 Tay Sachs 47 activating mutations 47 manic depression bipolar disorder 47 Dr. Bezprozvanny 47 NAFLD 47 Friedreich Ataxia 47 neurotransmission 47 #q# deletion syndrome 47 Insulin resistance 47 insulin resistance syndrome 47 glucocorticoid receptors 47 genomic imprinting 47 Li Huei Tsai 47 autoimmune disorder 47 vitamin B# deficiency 47 MYH9 gene 47 congenital hyperinsulinism 47 hemolytic anemia 47 Male pattern baldness 47 VIPR2 47 Hereditary angioedema 47 wet macular degeneration 47 Chronic constipation 47 chromosomal rearrangement 47 aneuploidy 47 Anxiety disorders 47 respiratory viral infections 47 Obstructive sleep apnea OSA 47 aspergers syndrome 47 Fabry disease 47 ciliopathies 47 Muscular dystrophies 47 subependymal giant cell 47 galanin 47 blood clotting disorder 47 TMEM#B 47 beta thalassemia 47 breast cancer metastasis 47 renovascular hypertension 47 inherited neurodegenerative 47 Dravet 47 sleep disorders 47 SGS# 47 compulsive hoarding 47 metabolic disorders 47 Attention Deficit Disorder ADD 47 neuro degenerative disorder 47 cataplexy 47 Congenital Adrenal Hyperplasia 47 Aortic stenosis 47 Morquio syndrome 47 Wolf Hirschhorn 47 neurologic diseases 47 dry scaly skin 47 demyelination 47 epidermolysis bullosa EB 47 Diabetic retinopathy 47 combined immunodeficiency SCID 47 dystonia 47 mental retardation 47 ichthyosis vulgaris 47 measles virus 47 PCNSL 47 hypertrophic cardiomyopathy 47 Chronic lymphocytic leukemia 47 motor neuron degeneration 47 CDH1 47 primary ovarian insufficiency 47 neurobiological 47 cognitive impairment 47 primary generalized tonic 47 herpes viruses 47 Hereditary angioedema HAE 47 dopamine D4 receptor 47 Juvenile Rheumatoid Arthritis 47 ADD ADHD 47 Gorlin syndrome 47 aneuploidies 47 habitual snoring 47 Haptoglobin 47 Canavan Disease 47 hyperactivity 47 ARID1A 47 Fetal alcohol 47 Hyperthyroidism 47 TNF blockers 47 idiopathic anaphylaxis 47 recurrent miscarriages 47 Attention deficit hyperactivity 47 Moebius syndrome 47 autistic 47 causative gene 47 severe congenital neutropenia 47 undiagnosed celiac disease 47 interstitial lung disease 47 autosomal recessive disorder 47 auditory processing 47 Neurofibromatosis 47 metabolic syndrome 47 atypical hemolytic uremic syndrome 47 Mild cognitive impairment 47 syndrome gastroesophageal reflux 47 familial hypercholesterolemia FH 47 chromosome abnormalities 47 Polycystic ovary syndrome PCOS 47 Maroteaux Lamy syndrome 47 tetrabenazine 47 dystrophin gene 47 retinitis pigmentosa RP 47 Narcolepsy 47 hypothalamic pituitary adrenal axis 47 biliary atresia 46 epigenetic mechanisms 46 NOMID 46 urea cycle 46 Parkinson disease PD 46 Alzheimer pathology 46 untreated celiac disease 46 bipolar disorder 46 long QT syndrome 46 Dwarfism 46 underlying molecular mechanisms 46 G#S [002] 46 GBA mutations 46 Cryptococcus neoformans 46 Fatty liver 46 Sexsomnia 46 myalgic encephalomyelitis ME 46 zinc deficiency 46 optic atrophy 46 Congenital Muscular Dystrophy 46 Irritable bowel syndrome 46 medulloblastoma tumors 46 remyelination 46 factor BDNF 46 progranulin 46 LKB1 46 Chronic Myeloid Leukemia 46 Parkinson Disease PD 46 metabotropic glutamate receptors 46 Bipolar disorder 46 Cowden syndrome 46 Hurler Syndrome 46 dysautonomia 46 genetic variants 46 genetic variation 46 von Hippel Lindau 46 vitamin D deficiency 46 congenital disorder 46 macular degeneration 46 Friedreich 46 endothelial dysfunction 46 Cholangiocarcinoma 46 LRRK2 mutation 46 generalized seizures 46 hepatitis B infection 46 leukemias lymphomas 46 Treg cell 46 Prematurity 46 alpha1 antitrypsin deficiency 46 Skp2 46 Alzheimer disease 46 incurable neurodegenerative disease 46 CIAS1 46 irritable bowel syndrome IBS 46 RSV infections 46 ORMDL3 46 Inflammatory bowel diseases 46 Adrenoleukodystrophy 46 RPE# gene 46 progeria rare 46 NPHP 46 Apert syndrome 46 Cystic fibrosis CF 46 locus coeruleus 46 autosomal recessive genetic 46 type 1diabetes 46 type1 diabetes 46 severe dehydrating diarrhea 46 Autism 46 psychiatric illnesses 46 Sjögren syndrome 46 folate deficiency 46 myelination disorders 46 Sandhoff disease 46 neuropsychiatric diseases 46 incurable genetic 46 Epstein Barr virus EBV 46 neuronal degeneration 46 Glioblastoma multiforme GBM 46 Myelodysplastic syndromes MDS 46 gastroesophageal reflux GERD 46 Morquio 46 APOE ε4 46 peanut allergy 46 chromosomal abnormalities 46 Infantile spasms 46 sensorineural hearing loss 46 #ß HSD1 46 complex neurobiological disorder 46 PPHN 46 presbyopia 46 Preeclampsia 46 Sickle cell 46 Hedgehog pathway 46 protein misfolding diseases 46 Systemic lupus erythematosus SLE 46 parkin gene 46 osteosarcoma bone 46 2 diabetes T2D 46 MLL2 46 PDGFRA 46 chromosomal disorders 46 diabetic retinopathy 46 genetic trait 46 Angelman 46 nonalcoholic steatohepatitis NASH 46 Inflammatory Bowel Disease 46 autosomal dominant polycystic kidney 46 alpha synuclein 46 IGF1 46 primary immunodeficiency 46 myotonia 46 ankyrin B 46 miRNA genes 46 DIPG 46 neurofibromas 46 related macular degeneration 46 Chronic fatigue syndrome 46 Oxidative stress 46 cerebral palsy Down syndrome 46 Dyslexia 46 tumor suppressor protein 46 myelin repair 46 bronchopulmonary dysplasia 46 manic episode 46 Acute Myelogenous Leukemia 46 airway hyperresponsiveness 46 endocrine disorder 46 INF2 46 monogenic 46 hedgehog pathway 46 alpha synuclein gene 46 heterozygous FH 46 beta amyloid plaques 46 narcolepsy 46 Krabbe leukodystrophy 46 disabling neurological 46 excitotoxicity 46 leukemias 46 Fasudil 46 NOTCH1 46 iron overload 46 cognitive disorders 46 Cancer cachexia 46 structural abnormalities 46 generalized epilepsy 46 Vitamin D deficiency 46 tumor suppressor genes 46 regulator CFTR gene 46 Sleep apnea 46 Von Hippel Lindau 46 p# mutations 46 JAK2 enzyme 46 Janus kinase 46 MC1R 46 Fibrosis 46 progranulin mutations 46 neuroendocrine 46 ADDLs 46 malignant hyperthermia 46 Obstructive Sleep Apnea OSA 46 RDEB 46 demyelinating disease 46 APOE4 gene 46 onset Alzheimer 46 neurological abnormalities 46 Chiari malformation 46 IgA nephropathy 46 systemic scleroderma 46 leukodystrophy 46 BRAF gene 46 dysbindin 46 acute myeloid leukemia AML 46 huntingtin protein 46 Asperger syndrome 46 hereditary disorders 46 gastroparesis 46 1 diabetes T1D 46 Anencephaly 46 acute lymphoblastic leukemia 46 calcineurin 46 restless legs 45 spasmodic dysphonia 45 congenital brain tumor 45 Folic acid deficiency 45 FGFR2 45 premutation 45 Migraine headaches 45 manic depressive illness 45 chromosomal aberrations 45 chromosomal defects 45 epigenetic modification 45 Crohn disease 45 hereditary nonpolyposis colon cancer 45 Neuregulin 1 45 alpha thalassemia 45 abnormal chromosome 45 retinal dysfunction 45 MGUS 45 LRRK2 mutations 45 primary ciliary dyskinesia 45 Diamond Blackfan anemia 45 TACI mutations 45 recessive inheritance 45 dilated cardiomyopathy 45 TGFBR1 * 6A 45 Zinc deficiency 45 PGTC seizures 45 fibrodysplasia ossificans progressiva 45 severe malignant osteopetrosis 45 aplastic anemia 45 SOD1 gene 45 Sturge Weber syndrome 45 Neurological disorders 45 epigenetic markers 45 gluten sensitivity 45 nonhereditary 45 progressive neurologic 45 heritable genetic 45 SMN2 45 disorders FASD 45 mental retardation epilepsy 45 metabolic disturbances 45 glutamate signaling 45 Nephrotic Syndrome 45 brain derived neurotrophic 45 GPR# [002] 45 Friedrich Ataxia 45 neuroinflammatory 45 Dravet Syndrome 45 MLH1 45 degenerative disorders 45 Diabetic neuropathy 45 Depressive disorders 45 Irlen Syndrome 45 microcephaly 45 Systemic lupus 45 fronto temporal dementia