Related by context. All words. (Click for frequent words.) 70 autosomal recessive 67 dominantly inherited 65 recessive genetic 64 neurodegenerative disorder 63 autosomal dominant 63 highly heritable 63 ataxias 63 genetic abnormality 62 inherited neurodegenerative 62 de novo mutations 61 holoprosencephaly 61 autosomal recessive disease 61 autosomal dominant disorder 61 recessive trait 61 Retinitis pigmentosa 61 incurable genetic 61 inherited mutations 61 inherited retinal degeneration 61 neuropsychiatric disorder 61 neurological disorder affecting 61 developmental abnormalities 61 chromosomal anomaly 61 fatal myelination disorder 61 fatal neurodegenerative 60 muscular dystrophy cystic fibrosis 60 HGPS 60 MYH9 gene 60 Lesch Nyhan syndrome 60 congenital disorders 60 progressive neurodegenerative disorder 60 Meckel Gruber 60 Hutchinson Gilford Progeria Syndrome 60 Spinal muscular atrophy 60 fatal neuromuscular disorder 60 genes predisposing 60 hereditary degenerative 60 multisystem disease 60 mitochondrial mutations 60 autosomal dominant inheritance 60 CHD7 60 familial adenomatous polyposis 60 Li Fraumeni syndrome 60 inherited neurological disorder 59 Genetic predisposition 59 Kufs disease 59 Cystic fibrosis CF 59 autosomal recessive disorder 59 hereditary spastic paraplegia 59 FTLD 59 Hashimoto thyroiditis 59 dysgenesis 59 cystic fibrosis sickle cell 59 maternally transmitted 59 nongenetic 59 chromosomal anomalies 59 Proteus syndrome 59 PTEN mutations 59 immuno deficiency 59 chromosomal disorders 59 Hutchinson Gilford progeria 59 lysosomal storage disease 59 heritable 59 AAT deficiency 59 Angelman syndrome 59 hereditary deafness 59 Brugada Syndrome 58 LRRK2 mutations 58 HNPCC 58 Alport syndrome 58 autosomal recessive genetic 58 Lafora disease 58 progressive neurodegenerative 58 Usher Syndrome 58 huntingtin gene 58 Proteus Syndrome 58 Dwarfism 58 Apert syndrome 58 hereditary predisposition 58 degenerative disorder 58 chromosomal alterations 58 Hereditary angioedema 58 polymorphic ventricular tachycardia 58 degenerative neurological disease 58 Male pattern baldness 58 Fragile X gene 58 mosaicism 58 monogenic 58 ADPKD 58 untreated celiac disease 58 chromosome abnormality 58 neurofibromas 58 apolipoprotein E gene 58 mental retardation epilepsy 58 chromosomal disorder 58 congenital deafness 58 Beta thalassemia 58 Prion diseases 58 hereditary nonpolyposis colorectal cancer 58 immunodeficiencies 58 Dilated cardiomyopathy 58 Tay Sachs disease 58 alpha thalassemia 58 causative gene 57 Becker muscular dystrophy 57 ectodermal dysplasia 57 spontaneous mutations 57 fatal neurodegenerative disorder 57 dyskeratosis congenita 57 Bardet Biedl Syndrome 57 hyperinsulinism 57 neurofibroma 57 genetic disorder 57 phenotypic expression 57 neurodevelopmental disorder 57 progressive degeneration 57 Marfan syndrome connective tissue 57 genetic defect 57 fronto temporal dementia 57 hydrops 57 severe malignant osteopetrosis 57 motor neuron degeneration 57 Maroteaux Lamy Syndrome 57 frontotemporal dementia 57 #q#.# deletion syndrome 57 CHARGE syndrome 57 FXTAS 57 phthalate syndrome 57 neurological abnormalities 57 nonhereditary 57 APOE ε4 57 Osteogenesis imperfecta 57 MC1R 57 progressive degenerative neurological 57 non syndromic 57 penetrance 57 neurobiological disorder 57 GBA mutations 57 spongiform encephalopathies 57 paraneoplastic 57 Polycystic kidney disease 57 susceptibility gene 57 SCA5 57 biochemical imbalance 57 Genetic mutations 57 Klinefelter Syndrome 57 hereditary disorder 57 Prader Willi syndrome 57 thyroiditis 57 genetic abnormalities 57 Dravet syndrome 56 Niemann Pick disease 56 Joubert syndrome 56 Leber hereditary optic neuropathy 56 monozygotic twins 56 familial polyposis 56 Medulloblastoma 56 Klinefelter syndrome 56 KIBRA 56 anatomical abnormalities 56 disabling neurological 56 persistent pulmonary hypertension 56 maternally inherited 56 mitochondrial disorders 56 clinically heterogeneous 56 childhood disintegrative disorder 56 Parkinsonian Syndromes 56 congenital 56 Neurofibromatosis type 56 Vascular dementia 56 Arrhythmogenic Right Ventricular Cardiomyopathy 56 primary ciliary dyskinesia 56 chromosomal defect 56 Pulmonary hypertension 56 Childhood Disorder 56 neuro developmental disorder 56 chronic autoimmune disorder 56 AAT Deficiency 56 lysosomal storage diseases 56 nondemented 56 predisposing factor 56 Von Hippel Lindau 56 inherited predisposition 56 pathophysiologic 56 skeletal dysplasia 56 incurable neurological disorder 56 inherited genetic mutations 56 herpesviruses 56 hypertrophic cardiomyopathy HCM 56 recessive mutations 56 Tuberous sclerosis 56 WAGR syndrome 56 cerebri 56 genetic defects 56 spinocerebellar ataxia 56 polydactyly 56 underlying pathophysiology 56 myopathies 56 chronic granulomatous disease 56 velo cardio facial 56 alexithymia 56 gene MECP2 56 sporadic ALS 56 mtDNA mutations 56 progressive neurodegenerative disease 56 causative genes 56 aetiological 56 JAK mutations 56 cystic fibrosis Duchenne muscular 56 cerebellar hypoplasia 55 microdeletion 55 abnormal chromosome 55 HFE gene 55 Coeliac disease 55 PTPN# 55 Myotonic dystrophy 55 autistic traits 55 neuro degenerative 55 Cowden syndrome 55 genetic predisposition 55 spastic paraplegia 55 impaired cognition 55 debilitating neurodegenerative disorder 55 Worthingtons testified 55 aniridia 55 Congenital Adrenal Hyperplasia 55 recessive genes 55 metabolic abnormality 55 Anorexia nervosa 55 proband 55 puerperal psychosis 55 cardiac channelopathies 55 genetic syndromes 55 Cockayne syndrome 55 von Hippel Lindau 55 IgA deficiency 55 Crouzon Syndrome 55 hereditary hemochromatosis 55 microcephalin 55 Muscular dystrophy 55 cause cardiac channelopathies 55 Meckel Gruber syndrome 55 cystic fibrosis muscular dystrophy 55 familial dysautonomia 55 Hyperthyroidism 55 Von Willebrand disease 55 nerve degeneration 55 brain malformation 55 autoinflammatory diseases 55 infertility miscarriage 55 Stargardt Macular Dystrophy 55 galactosemia 55 Fragile X Syndrome 55 fat malabsorption 55 retinal dysfunction 55 degenerative neurological diseases 55 MECP2 gene 55 hippocampal function 55 multisystem disorder 55 ataxia telangiectasia 55 blindness deafness 55 epidermolysis bullosa EB 55 Hutchinson Gilford Progeria 55 hormonal abnormalities 55 Sanfilippo Syndrome 55 thyroid hormone deficiency 55 pathognomonic 55 primitive neuroectodermal tumors 55 Leber congenital amaurosis 55 oligodendrogliomas 55 Tay Sachs genetic 55 leptin deficiency 55 chromosomal defects 55 autism dyslexia 55 achromatopsia 55 Aortic stenosis 55 sexually dimorphic 55 Sturge Weber syndrome 55 progressive degenerative 55 immunodeficiency disorder 55 undiagnosed celiac disease 55 CALHM1 55 aneuploidies 55 Retinopathy 55 Chlamydia pneumoniae 55 Lactose intolerance 55 degenerative neurological disorder 55 Usher syndrome 55 cone photoreceptors 55 neurocognitive dysfunction 55 congenital cataract 55 facioscapulohumeral muscular dystrophy 55 immunodeficiency 55 Wiskott Aldrich Syndrome 55 Hip dysplasia 55 FMRP protein 55 pancreatic endocrine 55 genetic imprinting 55 schizoid personality 55 susceptibility genes 55 auditory neuropathy 55 testicular tumors 55 Loeys Dietz syndrome 55 Genetic variants 55 Fanconi anemia 55 cystic kidney 55 heritable genetic 55 Atopic eczema 55 TTR amyloidosis 55 variable immunodeficiency 55 diseases chronic granulomatous 55 Cryptococcus neoformans 55 anosognosia 55 Atopic dermatitis 55 optic atrophy 55 sickle cell cystic fibrosis 55 autism Asperger 55 Severe Combined Immunodeficiency 55 Hypophosphatasia 55 biological predisposition 55 Motor neurone disease 55 mitochondrial defects 54 progressive neurodegenerative disorders 54 neurological dysfunction 54 predisposing 54 cardiac fibrosis 54 skeletal abnormalities 54 rheumatic disease 54 neonatal respiratory distress 54 lymphocytic 54 familial clustering 54 polyhydramnios 54 Pervasive Developmental Disorder 54 genetic makeups 54 genetic mutations 54 missense mutations 54 Crouzon syndrome 54 autoimmune thyroid 54 monozygotic twin 54 autoimmune thyroiditis 54 modifier genes 54 recessive inheritance 54 exfoliation glaucoma 54 ichthyosis vulgaris 54 multisystemic 54 TP# mutation 54 familial aggregation 54 inheritable genetic 54 mitochondrial myopathy 54 germline mutations 54 brain lesions 54 COMT gene 54 neurodevelopment disorder 54 systemic scleroderma 54 disorder ASD 54 autosomal dominant polycystic kidney 54 roseola 54 homocystinuria 54 incurable neurodegenerative disease 54 polydactylism 54 parkinsonian 54 neurofibrillary 54 NF1 54 Bacterial vaginosis 54 Leber congenital amaurosis LCA 54 osteogenesis imperfecta 54 degenerative neuromuscular disease 54 Chronic fatigue 54 APOE gene 54 unprovoked seizures 54 Sjögren syndrome 54 enteroviral 54 Vitamin B# deficiency 54 Wolf Hirschhorn 54 DRD2 gene 54 neuronal dysfunction 54 phenotypic variation 54 chromosomal aberration 54 Genetic variation 54 nephritis 54 hypotonia 54 autonomic nerve 54 ApoE gene 54 xeroderma pigmentosum 54 1 Antitrypsin Deficiency 54 genetic mutation 54 carbohydrate intolerance 54 debilitating neurodegenerative 54 hereditary disorders 54 APOE genotype 54 apolipoprotein E APOE 54 predispose 54 Inflammatory bowel diseases 54 common disabling neurological 54 leukodystrophies 54 channelopathies 54 Mitochondrial diseases 54 Oxidative stress 54 GABRA2 gene 54 prematurity ROP 54 microvascular disease 54 CNTNAP2 54 fibrous dysplasia 54 Zinc deficiency 54 chronic idiopathic 54 hypokalemia hypomagnesemia 54 DNA methylation patterns 54 Systemic lupus erythematosus SLE 54 narcolepsy cataplexy 54 systemic amyloidosis 54 histiocytosis 54 Nonalcoholic fatty liver 54 gastrointestinal dysfunction 54 Fanconi anemia FA 54 Joubert Syndrome 54 traumatic disabling neurological 54 sCJD 54 epigenetic changes 54 polygenic 54 motor neuron diseases 54 Hemiplegia 54 Beckwith Wiedemann syndrome 54 fibrodysplasia ossificans progressiva 54 NPHP 54 hereditary nonpolyposis colon cancer 54 microcephaly 54 Sanfilippo syndrome 54 CCR5 delta# 54 behavioral abnormalities 54 HIBM 54 metabolic abnormalities 53 Malignant mesothelioma 53 filaggrin gene 53 Polymorphic Ventricular Tachycardia CPVT 53 Oppositional Defiant Disorder 53 CFTR gene 53 bone deformities 53 neurological disorder characterized 53 Treg cell 53 pseudotumor cerebri 53 ciliopathies 53 C#Y 53 SHANK3 gene 53 related maculopathy 53 congenital glaucoma 53 Krabbe leukodystrophy 53 cystic fibrosis chronic pancreatitis 53 recessive gene 53 Autoimmune disorders 53 SSc 53 optic nerve hypoplasia 53 antiphospholipid syndrome 53 Rubinstein Taybi syndrome 53 inflammatory demyelinating 53 Vitamin D insufficiency 53 Celiac sprue 53 embryonic tissues 53 APOE4 53 idiopathic epilepsy 53 teratoma 53 DiGeorge syndrome 53 idiopathic PAH 53 filaggrin 53 predisposing factors 53 encephalitis swelling 53 Hereditary angioedema HAE 53 Porphyria 53 Muscular dystrophies 53 hyperplastic 53 chronicity 53 CDH1 53 CFH gene 53 dermatomyositis 53 Irritable bowel syndrome 53 G6PD deficiency 53 Fatty liver 53 hyper IgE syndrome 53 Frontal lobe 53 neuronal ceroid lipofuscinosis 53 MELAS 53 defective cilia 53 IL#R 53 Magnesium deficiency 53 gene locus 53 enterocolitis 53 APOE e4 53 chromosomal deletions 53 muscle degeneration 53 Diverticulosis 53 1 diabetes T1D 53 enteroviral infection 53 hemochromatosis 53 neurodegenerative disorder characterized 53 Peutz Jeghers syndrome 53 imperfecta 53 neurobehavioral disorder 53 giant danio 53 induced cardiomyopathy 53 necrotising 53 LIS1 53 deafness blindness 53 homozygosity 53 LQTS 53 structural abnormalities 53 schizotypal 53 myasthenia gravis MG 53 granulosa cell 53 lupus scleroderma 53 septo optic dysplasia 53 neurologic disorder 53 polycystic ovarian syndrome PCOS 53 presymptomatic 53 papillomaviruses 53 inherited neurodegenerative disorder 53 Tay Sachs thalassemia 53 pituitary tumors 53 dystrophies 53 Bardet Biedl syndrome 53 protozoan parasites 53 LMNA 53 degenerative retinal disease 53 chromosomal instability 53 familial pancreatic cancer 53 Bronchiolitis 53 chronic obstructive airway 53 genus Plasmodium 53 Hypertrophic cardiomyopathy 53 NKX2 53 orchitis 53 ENPP1 53 alexia 53 ceroid lipofuscinosis NCL 53 epididymitis 53 limb malformations 53 involuntary tics 53 inherit predisposition 53 CHRNA5 gene 53 dopamine receptor gene 53 genomic variants 53 allelic variation 53 BARD1 53 Mendelian disorders 53 Churg Strauss syndrome 53 Leydig cell 53 rheumatoid arthritis lupus 53 epigenetic alterations 53 CETP gene 53 microchimerism 53 syringomyelia 53 Lou Gehrigs disease 53 ADA SCID 53 PB1 F2 53 achondroplasia 53 genetically predetermined 53 chromosomal abnormality 53 susceptibility alleles 53 Jakob Disease 53 slow caffeine metabolizers 53 germline mutation 53 prosopagnosia 53 Alport Syndrome 53 chromosome deletion 53 prenatally diagnosed 53 Folic acid deficiency 53 Heritability 53 genetic underpinnings 53 MEF2A 53 heterotaxy 53 Iron deficiency anemia 53 pyloric stenosis 53 Essential tremor 53 paralysis blindness 53 Menkes disease 53 inappropriate antidiuretic hormone SIADH 53 inbred strains 53 urethritis 53 familial hypercholesterolemia 53 genetic trait 53 multi infarct dementia 53 obesity insulin resistance 53 heritable trait 53 Angelman Syndrome 53 epilepsies 53 body dysmorphic 52 G#S mutation 52 Marfan Syndrome 52 pathogenetic 52 retinitis pigmentosa hereditary 52 disorder characterized 52 MGUS 52 chronic relapsing 52 Henoch purpura 52 congenital anomaly 52 dementia praecox 52 Aspergers Syndrome 52 thalassemia sickle cell 52 neurological degeneration 52 interferon pathway 52 vasopressin receptors 52 degenerative neurological 52 familial adenomatous polyposis FAP 52 retinitis pigmentosa RP 52 haemochromatosis 52 idiopathic generalized epilepsy 52 amusia 52 endocrine disorder 52 neurocysticercosis 52 neurologic disorders 52 Rh incompatibility 52 spinal muscle atrophy 52 molecular abnormalities 52 #q#.# [001] 52 abnormalities 52 mitochondrial dysfunction 52 Inflammatory bowel disease 52 asperger syndrome 52 Abnormalities 52 frontotemporal 52 Amyotrophic lateral sclerosis 52 post transplant lymphoproliferative 52 osteogenesis imperfecta OI 52 arthritis lupus 52 sporadic Creutzfeldt Jakob 52 deletion 5q 52 neurofibromatosis type 52 TCF#L# gene 52 juvenile idiopathic arthritis JIA 52 tricuspid atresia 52 heredity 52 p# mutations 52 progeria rare 52 insulin resistance syndrome 52 McCune Albright 52 genetic determinants 52 encephalitis inflammation 52 HLA DRB1 * 52 insulin secreting beta 52 inborn 52 comorbid disorders 52 Hypospadias 52 Down syndrome chromosomal disorder 52 congential 52 gastric carcinoma 52 neuro degenerative disorder 52 Korsakoff syndrome 52 disorder FASD 52 robs sufferers 52 atypical hemolytic uremic syndrome 52 Hurler syndrome 52 dopamine transporter gene 52 spinocerebellar ataxia type 52 NPM1 gene 52 skeletal muscle weakness 52 encephalitis meningitis 52 #q# deletion 52 Nicotine dependence 52 Hypertensive heart 52 BMPR2 52 degenerative disorders 52 severe dehydrating diarrhea 52 advanced glycation endproducts 52 Myasthenia gravis 52 DQB1 * 52 MYH9 52 Pompe Disease 52 MSH2 52 basal cell nevus syndrome 52 Stargardt Macular Dystrophy SMD 52 LRRK2 gene 52 retinal blindness 52 chronic hepatitis cirrhosis 52 inbreeding depression 52 genetic alterations 52 mutation 52 exotropia 52 chromosomal rearrangement 52 Diabetic neuropathy 52 nonsense mutations 52 lichen planus 52 pathophysiological 52 heritable variation 52 dissecans 52 retinitis 52 degenerative muscular 52 Perthes disease 52 Cerebral malaria 52 Toxoplasmosis 52 bone marrow mesenchymal stem 52 associated tremor ataxia 52 Alleles 52 Marfan Syndrome connective tissue 52 incurable degenerative 52 behavioral disinhibition 52 rare chromosomal disorder 52 familial ALS 52 androgenic alopecia 52 incurable neurological 52 unknown etiology 52 EBV infection 52 chronic lymphocytic 52 Eosinophilic esophagitis 52 cerebellar 52 Chronic pancreatitis 52 recessive mutation 52 spontaneous mutation 52 atopic disorders 52 spastic diplegia 52 Krabbe Disease 52 Dysplasia 52 causally linked 52 corneal dystrophy 52 missense mutation 52 hyperexcitability 52 Gluten intolerance 52 Huntington Chorea 52 Asperger syndrome milder 52 nonseminoma 52 lateral sclerosis ALS 52 myelogenous leukemia 52 myeloproliferative neoplasms 52 Ehlers Danlos syndrome 52 Leukemias 52 dysmorphic features 52 SLC#A# gene [002] 52 lysosomal diseases 52 genetic susceptibility 52 autonomic dysfunction 52 hypercoagulability 52 defective gene 52 Premature Aging 52 malformations 52 dysmorphic 52 congenital abnormalities 52 maladaptive 52 debilitating neuromuscular 52 Down syndrome spina bifida 52 ischemic optic neuropathy 52 bullous 52 polyglutamine diseases 52 anemias 52 familial hypercholesterolemia FH 52 RET PTC rearrangements 52 myeloproliferative 52 Genetic mutation 52 Burkholderia 52 BRAF V#E 52 Excessive daytime sleepiness 52 Compulsive hoarding 52 sclerosis ALS 52 congenital deficiency 52 G#S [002] 52 Fragile X syndrome 52 genetic lysosomal storage 52 Sporadic CJD 52 Degenerative diseases 52 generalized epilepsy 52 hereditary blindness 52 Parkinson disease neurological disorder 52 irreversible blindness 52 inherited retinal 52 retinal vascular 52 Mendelian 52 Congenital heart 52 fatal neuromuscular 52 Alzheimer Disease AD 52 FASPS 52 tapeworm infection 52 amyloid cascade 52 idiopathic 52 systemic mastocytosis 52 prostate carcinogenesis 52 fibromatosis 52 hereditary hemorrhagic telangiectasia 52 Endometrial cancer 52 Arrhythmogenic 52 MLH1 52 etiologic 52 myalgic encephalomyelitis ME 52 embryonal rhabdomyosarcoma 52 Mild cognitive impairment 52 Fetal alcohol 52 heritable diseases 52 dizygotic twins 52 pulmonary metastasis 52 Schizoaffective Disorder 52 immunodeficient 52 Hirschsprung disease 52 CYP#C# gene 52 neuropsychological functioning 52 beta thalassemia 52 celiac sprue 52 C. pneumoniae 52 myelitis 52 Parkinsons disease 52 plexiform 52 hypogonadotropic hypogonadism 52 neurological sequelae 52 Genetic variations 52 obstructive coronary artery 51 VHL gene 51 Brugada syndrome 51 meningitis encephalitis 51 KCNQ1 51 Glioblastomas 51 HLA B# 51 blindness paralysis 51 genetic variation 51 eosinophilic 51 oculomotor 51 OPRM1 gene 51 agnosia 51 chromosomal imbalance 51 alveolar rhabdomyosarcoma 51 Marfan syndrome 51 vWD 51 leaky gut 51 Nasal allergies 51 progranulin mutations 51 ABCB1 gene 51 MTHFR 51 Glioblastoma multiforme GBM 51 autoinflammatory 51 Inappropriate activation 51 Myocarditis 51 V Leiden 51 hematologic disorders 51 polymyalgia rheumatica 51 Foxp2 51 osteopetrosis 51 alpha1 antitrypsin deficiency 51 ANCA associated 51 tremors slowness 51 SORL1 gene 51 hematological abnormalities 51 multiple sclerosis epilepsy 51 FGFs 51 biochemical imbalances 51 leukodystrophy 51 Bullous 51 Viral infections 51 hyperprolactinemia 51 genetically predisposed 51 neural crest 51 abnormal chromosomes 51 genetically susceptible 51 erythematosus 51 schizophreniform disorder 51 heritable disorders 51 severe congenital neutropenia 51 KRAS oncogene 51 polymicrobial 51 multiply uncontrollably 51 lymphoid cells 51 euthymic patients 51 Prenatal diagnosis 51 Gliomas 51 internalizing disorders 51 thrombophilia 51 metabolic dysfunction 51 diabetic retinopathy DR 51 Wiskott Aldrich syndrome 51 nonalcoholic steatohepatitis NASH 51 cryptogenic 51 NF1 gene 51 allergic eczema 51 Cognitive impairment 51 incurable degenerative brain 51 Apert 51 dopamine signaling 51 vascular cognitive impairment 51 Suicidal tendencies 51 MC1R gene 51 herpes simplex encephalitis 51 strep bacteria 51 hepatic renal 51 Diabetic retinopathy 51 leukoencephalopathy 51 Mitral regurgitation 51 multifactorial disease 51 Fanconi anemia rare 51 homozygous FH 51 Raynaud syndrome 51 lethal arrhythmias 51 e4 allele 51 assortative mating 51 CAG repeats 51 cryptorchidism 51 mutations 51 mitochondrial DNA mutations 51 glutamic acid decarboxylase 51 metachromatic leukodystrophy 51 bronchopulmonary dysplasia 51 predisposes 51 Asberger syndrome 51 Maroteaux Lamy syndrome 51 leiomyoma 51 astrocytomas 51 Polycystic ovary syndrome 51 MC4R gene 51 Dental fluorosis 51 Cleft lip 51 gastric carcinomas 51 inhibitory transmitter 51 MMP# 51 Malassezia 51 breast endometrial 51 NF2 51 neurobiological basis 51 pituitary adenoma 51 susceptibility locus 51 hyperparathyroidism 51 schizotypal traits 51 Periodontal disease 51 blastoma 51 etiologic factors 51 recessively inherited 51 neuroinflammation 51 Myocardial infarction 51 aortic atherosclerosis 51 JAK2 mutation 51 aciduria 51 Entamoeba 51 androgenetic alopecia 51 spinal muscular atrophy SMA 51 aplasia 51 myopia nearsightedness 51 Androgenetic alopecia 51 autosomal 51 cystic fibrosis hereditary 51 pilocytic astrocytomas 51 disorders ASD 51 mutant gene 51 obsessive compulsive behaviors 51 methylenetetrahydrofolate reductase 51 erythema nodosum 51 Severe Primary IGFD 51 neuroblastomas 51 fusiform 51 chromosomal translocations 51 Anencephaly 51 spastic colon 51 Systemic lupus erythematosus 51 lactase deficiency 51 congenital adrenal hyperplasia 51 Creutzfeld Jakob disease 51 TACI mutations 51 oncogene addiction 51 congenital abnormality 51 APOE e4 gene 51 Hemangiomas 51 Premature Ovarian Failure 51 untreated hypothyroidism 51 APOE4 gene 51 causative mutations 51 overactive thyroid gland 51 Carcinoid tumors 51 synovial cells 51 fungoides 51 blood clotting disorders 51 Lewy body 51 fibrodysplasia ossificans progressiva FOP 51 Overactive 51 elevated triglyceride levels 51 Retinoblastoma 51 congenital diaphragmatic hernia 51 nonischemic 51 Pervasive Developmental Disorders 51 ADAMTS# 51 NASH Huntington 51 Variant Creutzfeldt Jakob 51 T. vaginalis 51 neurodevelopmental disorder characterized 51 Cerebral palsy 51 Chronic lymphocytic leukemia 51 Creutzfeldt Jacob 51 #q# deletion syndrome 51 epilepsy Parkinson disease 51 Huntingtons disease 51 sub syndromal 51 leiomyomas 51 genital abnormalities 51 rare autosomal recessive 51 meningeal 51 Pulmonary fibrosis 51 herpes encephalitis 51 disorder thalassemia 51 comorbid psychiatric 51 neurological manifestations 51 Oxidative damage 51 sarcoid 51 metabolic disorder 51 mito 51 tau pathology 51 ataxia 51 Schizoaffective disorder 51 Chronic lymphocytic leukemia CLL 51 aspergers 51 β thalassemia 51 Crigler Najjar syndrome 51 Psoriatic arthritis