Related by context. All words. (Click for frequent words.) 70 Dravet syndrome 69 Joubert syndrome 69 degenerative disorder 68 chromosomal disorder 68 holoprosencephaly 67 Fanconi anemia 66 brain malformation 66 NF1 66 Angelman Syndrome 66 Rett syndrome 66 neurodegenerative disorder 66 myotonic dystrophy 66 Hutchinson Gilford progeria 66 dyskeratosis congenita 66 chromosome abnormality 65 cerebellar hypoplasia 65 spastic diplegia 65 degenerative neurological disorder 65 autosomal recessive 65 incurable neurological disorder 64 Usher Syndrome 64 apraxia 64 ectodermal dysplasia 64 Rubinstein Taybi syndrome 64 CHARGE syndrome 64 genetic disorder 64 progressive neurodegenerative disorder 64 mitochondrial dysfunction 64 autosomal dominant 64 neurodevelopment disorder 64 osteogenesis imperfecta 64 Apert syndrome 64 Muscular dystrophy 64 septo optic dysplasia 63 Sandhoff disease 63 NF2 63 arthrogryposis 63 rare chromosomal disorder 63 juvenile myelomonocytic leukemia 63 HGPS 63 FXTAS 63 fibrodysplasia ossificans progressiva FOP 63 dominantly inherited 63 Pervasive Developmental Disorder 63 mitochondrial disease 63 Hurler syndrome 62 Sanfilippo Syndrome 62 static encephalopathy 62 Leber congenital amaurosis 62 inherited neurological disorder 62 de novo mutations 62 fatal neurodegenerative disorder 62 neurobiological disorder 62 inherited retinal degeneration 62 DiGeorge syndrome 62 Neurofibromatosis type 62 Fragile X Syndrome 62 Spinal muscular atrophy 62 spinocerebellar ataxia 62 Hurler Syndrome 62 ataxia 62 neurodevelopmental disorder 62 Cockayne syndrome 62 WAGR syndrome 62 Proteus syndrome 62 Becker muscular dystrophy 62 genetic defect 62 neuropsychiatric disorder 62 autosomal recessive genetic 62 hippocampal function 62 blastoma 62 Crouzon Syndrome 62 optic nerve hypoplasia 62 mitochondrial myopathy 62 Aspergers Syndrome 61 hereditary spastic paraplegia 61 Beckwith Wiedemann syndrome 61 Aspergers syndrome 61 Hirschsprung disease 61 RPE# 61 VCFS 61 Cerebral palsy 61 Myotonic dystrophy 61 Aicardi syndrome 61 Apert 61 achondroplasia 61 Fanconi Anemia 61 Myasthenia gravis 61 Obsessive compulsive disorder 61 Rett Syndrome 61 syringomyelia 61 neurodevelopmental 61 Asperger Disorder 61 epidermolysis bullosa EB 61 ataxia telangiectasia 61 degenerative neurological disease 61 Retinoblastoma 61 DiGeorge Syndrome 61 MECP2 gene 61 mental retardation epilepsy 61 neurological disorder affecting 61 Hashimoto thyroiditis 61 galactosemia 61 Meckel Gruber 61 Lafora disease 61 Kufs disease 61 Hutchinson Gilford Progeria 61 Childhood Disorder 60 Leber Congenital Amaurosis LCA 60 dystrophy 60 recessive genetic 60 Niemann Pick disease 60 inherited mutations 60 medium chain acyl 60 #q#.# deletion syndrome 60 neurofibromatosis type 60 embryonal rhabdomyosarcoma 60 neuro degenerative disorder 60 mutated gene 60 congenital disorder 60 chiari malformation 60 ataxias 60 hypotonia 60 autism neurological disorder 60 Friedreich ataxia 60 neuroblastomas 60 Noonan Syndrome 60 FTLD 60 hereditary blindness 60 hemophagocytic lymphohistiocytosis 60 neuro developmental disorder 60 primitive neuroectodermal tumors 60 medulloblastoma 60 microdeletion 60 autosomal dominant disorder 60 pseudotumor cerebri 60 hematological abnormalities 60 autosomal recessive disease 60 Medulloblastoma 60 prosopagnosia 60 chromosomal anomaly 60 Joubert Syndrome 60 synaptic function 60 incurable genetic 60 developmental abnormalities 60 chromosomal defect 60 autism spectrum disorders 60 Leber hereditary optic neuropathy 60 fatal neuromuscular disorder 60 ependymoma 59 Krabbe Disease 59 spastic paraplegia 59 cortical dysplasia 59 Beckwith Wiedemann Syndrome 59 Rett syndrome neurological disorder 59 generalized epilepsy 59 Lesch Nyhan syndrome 59 progressive neurological disorder 59 CDH1 59 chromosome deletion 59 fatal neurodegenerative 59 behavioral abnormalities 59 Li Fraumeni syndrome 59 genetic abnormality 59 Tay Sachs disease 59 Parkinson degenerative 59 Diamond Blackfan anemia 59 Asperger Syndrome AS 59 lissencephaly 59 dyspraxia 59 Essential tremor 59 achromatopsia 59 dysgenesis 59 spastic cerebral palsy 59 Krabbe Leukodystrophy 59 G#S mutation 59 spinal muscular atrophy 59 retinal degeneration 59 chromosomal abnormality 59 developmental disorders 59 Pompe Disease 59 mitochondrial disorders 59 chronic granulomatous disease 59 Wolf Hirschhorn 59 autistic tendencies 59 Parkinsons disease 59 Klinefelter syndrome 59 Oppositional Defiant Disorder 59 neurological dysfunction 59 mosaicism 59 Alport syndrome 59 genetically inherited 59 retinal dysfunction 59 hereditary hemorrhagic telangiectasia 59 juvenile dermatomyositis 59 sporadic ALS 59 Sanfilippo syndrome 58 Leber congenital amaurosis LCA 58 cerebellar ataxia 58 Langerhans Cell Histiocytosis 58 Proteus Syndrome 58 familial ALS 58 multisystem disorder 58 Progeria 58 hereditary disorder 58 genetic syndromes 58 Von Willebrand disease 58 rhabdomyosarcoma 58 dystonia neurological movement 58 immunodeficiency disorder 58 dysautonomia 58 Fragile X syndrome 58 gene MECP2 58 Asperger syndrome milder 58 recessive trait 58 savant syndrome 58 epidermolysis bullosa 58 Angelman 58 ADPKD 58 Holoprosencephaly 58 Prader Willi syndrome 58 biliary atresia rare 58 progranulin mutations 58 Chronic fatigue 58 involuntary tics 58 Chiari malformation 58 Severe Combined Immunodeficiency 58 childhood disintegrative disorder 58 immunodeficiencies 58 bronchopulmonary dysplasia 58 myasthenia gravis 58 FASPS 58 lymphoblastic leukemia 58 hypogonadotropic hypogonadism 58 Diamond Blackfan Anemia 58 Porphyria 58 paraneoplastic 58 Wiskott Aldrich Syndrome 58 hereditary deafness 58 disorders ASD 58 MELAS 58 quadriplegic cerebral palsy 58 Kleine Levin 58 fibrous dysplasia 58 skeletal dysplasia 58 dyscalculia 58 congenital deafness 58 Pelizaeus Merzbacher disease 58 complex neurobiological disorder 58 neuronal dysfunction 58 metachromatic leukodystrophy 58 tuberous sclerosis complex 58 muscular dystrophy 58 CHD7 57 Motor neurone disease 57 degenerative muscular 57 xeroderma pigmentosum 57 congenital muscular dystrophy 57 neurofibromatosis 57 disorder FASD 57 hypertrichosis 57 neuroendocrine 57 Bardet Biedl syndrome 57 disorder ASD 57 Duchenne muscular dystrophy 57 Autistic Disorder 57 autism 57 inherited neurodegenerative 57 incurable neurodegenerative disease 57 degenerative neurological condition 57 Ehlers Danlos syndrome 57 Wiskott Aldrich syndrome 57 congenital diaphragmatic hernia 57 ceroid lipofuscinosis NCL 57 muscle degeneration 57 biliary atresia 57 Coeliac disease 57 metabolic disorder 57 progressive degenerative neurological 57 Wilms tumor 57 congenital disorders 57 Cushing syndrome 57 hypothalamic hamartoma 57 neuroblastoma 57 ASDs 57 arthrogryposis multiplex congenita 57 hemiplegia 57 Treacher Collins 57 nonhereditary 57 neurodegenerative disease 57 CNTNAP2 57 Rhabdomyosarcoma 57 cognitive deficits 57 Neuregulin 1 57 undiagnosed celiac disease 57 Maroteaux Lamy Syndrome 57 polycystic kidney disease 57 retinitis pigmentosa RP 57 aneuploidies 57 Biliary atresia 57 autoinflammatory diseases 57 lysosomal storage disease 57 Apert Syndrome 57 medulloblastomas 57 Sonic Hedgehog 57 Lou Gehrigs disease 57 Alzheimers disease 57 neuritic 57 dysregulated 57 leukoencephalopathy 57 Epidermolysis bullosa 57 Duchene muscular dystrophy 57 neurological disorder 57 Brugada Syndrome 57 autosomal recessive disorder 57 spasmodic dysphonia 57 cerebral palsy 57 neurogenetic 57 tics involuntary 57 neurofibromatosis genetic disorder 57 Leber Hereditary Optic Neuropathy 57 Morquio syndrome 56 neurofibroma 56 Genetic predisposition 56 autosomal dominant polycystic kidney 56 Hutchinson Gilford Progeria Syndrome 56 immunodeficiency 56 Cowden syndrome 56 PKU genetic 56 aphasia 56 severe congenital neutropenia 56 neuropsychiatric disorders 56 Dwarfism 56 Aplastic anemia 56 LRRK2 gene 56 leukodystrophy 56 motor neuron diseases 56 progressive degeneration 56 alveolar rhabdomyosarcoma 56 autistic spectrum 56 neuroblastoma tumor 56 Alport Syndrome 56 demyelination 56 cerebellar 56 von Hippel Lindau 56 cortical plasticity 56 Retinitis pigmentosa 56 neurofibrillary 56 velo cardio facial 56 Usher syndrome 56 hydrops 56 Tuberous sclerosis 56 chronic autoimmune disorder 56 progeria rare 56 FMR1 gene 56 fronto temporal dementia 56 Spina bifida 56 lysosomal storage diseases 56 verbal apraxia 56 enzyme deficiency 56 cerebral palsy neurological disorder 56 Parkinsons Disease 56 Hypoplastic Left Heart 56 McCune Albright 56 Langerhans cell histiocytosis 56 Neurofibromatosis Type 56 neurodegenerative disorder characterized 56 Tourette Syndrome neurological disorder 56 NPHP 56 auditory neuropathy 56 neurodevelopmental disorders 56 Fanconi Anaemia 56 autism spectrum disorder 56 Parkinson disease degenerative 56 Ataxia 56 auditory processing 56 diaphragmatic hernia 56 Korsakoff syndrome 56 neurodevelopmental disorder characterized 56 polycystic kidneys 56 enterocolitis 56 dysphasia 56 Marfan syndrome connective tissue 56 Peutz Jeghers syndrome 56 congenital adrenal hyperplasia CAH 56 degenerative disease 56 progressive neurologic 56 Lennox Gastaut Syndrome 56 degenerative neuromuscular disease 56 autosomal dominant inheritance 56 underlying pathophysiology 56 Mitochondrial disease 56 progressive neurodegenerative 56 polycystic disease 56 Arnold Chiari Malformation 56 phonic tics 56 Parkinson disease neurodegenerative disorder 56 Krabbe disease 56 progressive neurodegenerative disease 56 Fragile X gene 56 aneuploidy 56 DiGeorge syndrome rare 56 autism Asperger 56 developmental disorder 56 Fanconi 56 gastrointestinal dysfunction 56 chromosomal translocations 56 MCAD deficiency 56 dopamine signaling 56 asperger syndrome 56 Treacher Collins syndrome 56 ocular albinism 56 congenital blindness 56 epilepsy 56 muscular dystrophies 56 roseola 56 neurodegeneration 56 experimental autoimmune encephalomyelitis 56 SHANK3 56 Smith Magenis syndrome 56 synaptogenesis 56 Ewing sarcoma bone 56 frontotemporal dementia 56 cerebral palsy epilepsy 56 Wilms Tumor 56 ASD autism spectrum 56 truncus arteriosus 56 MC1R 56 cardiac hypertrophy 56 debilitating neurodegenerative disorder 56 sacral agenesis 56 Congenital Adrenal Hyperplasia 56 amyloid cascade 56 autistic traits 56 Asperger 56 SAPAP3 56 Aspergers 56 myelomeningocele 56 Tourette syndrome neurological disorder 56 Krabbe leukodystrophy 56 Capgras 56 dissociative disorders 56 lymphoblastic lymphoma 56 STAT4 56 dysgraphia 56 Joubert syndromes 55 DISC1 gene 55 Polycystic kidney disease 55 KIBRA 55 Leber Congenital Amaurosis 55 Down syndrome 55 spinocerebellar ataxia type 55 inflammatory demyelinating 55 synaesthesia 55 microcephaly 55 Parkinsonian 55 spastic quadriplegic cerebral palsy 55 neuromuscular disease 55 MC4R gene 55 autoimmune encephalitis 55 progressive degenerative 55 Tourette Syndrome TS 55 retinitis pigmentosa degenerative 55 congenital cataract 55 nonsense mutation 55 mammary gland tumors 55 Moebius syndrome 55 developmental delays 55 neuronal degeneration 55 Osteosarcoma 55 synaptic plasticity 55 mitochondrial disorder 55 alzheimer disease 55 Kabuki syndrome 55 degenerative neurological diseases 55 Sjögren syndrome 55 Chiari Malformation 55 cystic fibrosis Duchenne muscular 55 diffuse intrinsic pontine glioma 55 REM sleep behavior 55 thunderclap headache 55 systemic amyloidosis 55 retinal dystrophy 55 CdLS 55 motor neurone 55 Pompe disease rare 55 Cryptococcus neoformans 55 acute colitis 55 multisystemic 55 spontaneous remission 55 DQB1 * 55 PANDAS 55 Wernicke Korsakoff syndrome 55 JMML 55 limb girdle muscular dystrophy 55 Wilm Tumor 55 renal fibrosis 55 Chronic constipation 55 mitochondrial mutations 55 genetic mutation 55 Crouzon syndrome 55 Six3 55 Dravet Syndrome 55 comorbid anxiety 55 leukodystrophies 55 von Willebrand disease 55 Diffuse Intrinsic Pontine Glioma 55 disabling neurological 55 genetic defects 55 progeria 55 autoimmune thyroiditis 55 SHANK3 gene 55 hyperemesis 55 Chronic Inflammatory Demyelinating Polyneuropathy 55 ectopic expression 55 Parkinson disease neurological disorder 55 genetic lysosomal storage 55 myalgic encephalomyelitis ME 55 Osteogenesis imperfecta 55 monozygotic twin 55 epigenetic changes 55 histrionic personality 55 neurological abnormalities 55 idiopathic generalized epilepsy 55 Rh incompatibility 55 dopamine D4 receptor 55 myelodysplasia 55 adult neurogenesis 55 osteopetrosis 55 Crigler Najjar syndrome 55 Hirschsprung Disease 55 pyloric stenosis 55 mastocytosis 55 dissociative amnesia 55 situs inversus 55 dysmorphic features 55 Tourette syndrome 55 spinal muscular atrophy SMA 55 Hyperactivity 55 hyperactivation 55 Dyspraxia 55 cystic kidney 55 SMN1 55 variable immunodeficiency 55 DICER1 55 Long QT syndrome 55 dermatomyositis 55 neurological disorder characterized 55 immuno deficiency 55 epigenetic alterations 55 Duchene Muscular Dystrophy 55 ataxic 55 mice lacking 55 chromosomal rearrangements 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 neurocysticercosis 55 Goldenhar Syndrome 55 IL#R 55 MCADD 55 demyelinating disease 55 Henoch purpura 55 hypophosphatasia 55 Brugada syndrome 55 manic depressive disorder 55 Marfan Syndrome connective tissue 55 neurofibromas 55 muscular dystrophy cystic fibrosis 55 beta thalassemia 55 Dysplasia 55 cerebri 55 mutant gene 55 spastic paralysis 55 nonsense mutations 55 plasticity 55 alexithymia 55 Diabetic neuropathy 55 gene mutation 55 medulloblastoma tumors 55 cause cardiac channelopathies 55 intractable epilepsy 55 diabetes insipidus 55 missense mutations 55 PDGFR 55 TMEM#B 55 spina bifida cerebral palsy 55 Spasticity 55 fatal myelination disorder 55 Hypophosphatasia 55 APOE gene 55 polydactylism 55 eosinophilic esophagitis 55 ANCA associated 55 Parkinsonism 55 neural crest 55 severe aplastic anemia 55 dystonia 55 myopathies 55 dysregulation 55 adrenal function 55 hereditary degenerative 54 primary biliary cirrhosis 54 cerebral palsy Down syndrome 54 lactase deficiency 54 ichthyosis 54 Neurogenesis 54 Apraxia 54 Prion diseases 54 recessive mutation 54 Meckel Gruber syndrome 54 alexia 54 frontotemporal 54 Dravet 54 familial adenomatous polyposis 54 syndrome FAS 54 nerve degeneration 54 Nf1 54 nephritis 54 microchimerism 54 Asberger syndrome 54 onset Alzheimer 54 epilepsies 54 idiopathic epilepsy 54 motor neuron disease 54 retinitis pigmentosa 54 Perthes disease 54 excitotoxicity 54 PTPN# 54 chromosomal rearrangement 54 Marfan 54 tuberous sclerosis 54 metabolic abnormalities 54 aniridia 54 nonalcoholic cirrhosis 54 lichen planus 54 Dysregulation 54 ciliopathies 54 debilitating neurological disease 54 hypothalamic pituitary adrenal axis 54 Hyperthyroidism 54 heritable 54 Borderline personality 54 impaired cognition 54 post transplant lymphoproliferative 54 neurological impairments 54 mito 54 LKB1 54 BMPR2 54 Erb palsy 54 paresis 54 chromosomal disorders 54 mitochondrial diseases 54 Goldenhar syndrome 54 polycystic ovary syndrome 54 juvenile myoclonic epilepsy 54 pathophysiologic 54 EBV infection 54 cognitive dysfunction 54 osteogenesis imperfecta OI 54 monogenic 54 Down syndrome cerebral palsy 54 Huntington Chorea 54 progressive retinal degenerative 54 interferon pathway 54 airway hyperresponsiveness 54 tau pathology 54 chromosome abnormalities 54 neuromotor 54 LIS1 54 Fanconi anemia rare 54 APOE4 54 cystic fibrosis hereditary 54 rheumatic disease 54 CNTNAP2 gene 54 Atopic dermatitis 54 systemic scleroderma 54 Asperger disorder 54 multisystem disease 54 persistent pulmonary hypertension 54 Chronic ITP 54 schizotypal 54 causative gene 54 VHL gene 54 Retinitis Pigmentosa RP 54 pulmonary atresia 54 missense mutation 54 seizure disorders 54 Attention Deficit Hyperactive Disorder 54 autism dyslexia 54 COMT gene 54 Autism Spectrum Disorder 54 FMRP protein 54 Cardiomyopathy 54 Klinefelter Syndrome 54 combined immunodeficiency SCID 54 facioscapulohumeral muscular dystrophy 54 associated tremor ataxia 54 Mitochondrial diseases 54 hyperinsulinism 54 frontotemporal dementia FTD 54 atypical hemolytic uremic syndrome 54 SMN protein 54 Mitochondrial 54 Moebius Syndrome 54 T1DM 54 juvenile rheumatoid arthritis 54 Tourette 54 myotonia 54 onset Alzheimer disease 54 abnormal chromosome 54 persistent genital arousal 54 Neurofibromatosis 54 Pulmonary hypertension 54 genetic neuromuscular disorder 54 hyperinsulinemia 54 myositis 54 teratoma 54 Niemann Pick 54 paraganglioma 54 fibromatosis 54 dilated cardiomyopathy 54 Purkinje cells 54 Marfan Syndrome 54 chronic lymphocytic 54 systemic mastocytosis 54 muscle wasting 54 Lennox Gastaut syndrome 54 myelogenous leukemia 54 pigmentosa 54 hypometabolism 54 podocytes 54 Cockayne Syndrome 54 mental retardation cerebral palsy 54 myoclonus 54 neurological 54 Male pattern baldness 54 Autoimmune disorders 54 progressive neuromuscular 54 1 diabetes T1D 54 Alzheimer Disease AD 54 rhabdomyosarcoma rare 54 Leydig cell 54 histiocytosis 54 AAT deficiency 54 Bardet Biedl Syndrome 54 EoE 54 parkinsonism 54 lymphocyte activation 54 obsessive compulsive disorder OCD 54 mood dysregulation 54 Ets2 54 intestinal inflammation 54 Major depressive disorder 54 Smad3 54 ependymomas 54 aspergers syndrome 54 airway remodeling 54 Cystic fibrosis CF 54 euthymic patients 54 overactivity 54 Sudden Arrhythmic Death 54 motor neuron degeneration 54 LQTS 54 Generalized anxiety disorder 54 HbF 54 biochemical imbalance 54 parkin gene 54 dysmotility 54 RDEB 54 Aicardi Syndrome 54 Down syndrome chromosomal disorder 54 dysarthria 54 dementia praecox 54 DIPG 54 DNA methylation patterns 54 craniosynostosis 54 chromosomal defects 54 coprolalia 54 common disabling neurological 54 diffuse pontine glioma 54 leukemia ALL 54 spinal bifida 54 Mental retardation 53 postoperative delirium 53 #q#.# [001] 53 APOE ε4 53 LRP5 53 Amyotrophic lateral sclerosis ALS 53 blindness deafness 53 SOD1 protein 53 Wegener granulomatosis 53 trisomy 53 Retinopathy 53 retinitis pigmentosa hereditary 53 Duchenne muscular dystrophy DMD 53 retrograde amnesia 53 phenotype 53 neuronal plasticity 53 recessively inherited 53 limb deformities 53 Wilms Tumour 53 Morquio Syndrome 53 petit mal seizures 53 IRS1 53 Parkinson Disease PD 53 Congenital Muscular Dystrophy 53 Polycystic ovary syndrome PCOS 53 motor neuropathy 53 Hereditary angioedema HAE 53 Li Huei Tsai 53 aspergers 53 insulin secreting beta 53 Cerebellar 53 spinal muscle atrophy 53 phthalate syndrome 53 brain lesions 53 hereditary nonpolyposis colorectal cancer 53 tic disorder 53 polymyalgia 53 nerve palsy 53 Tuberous Sclerosis 53 Anencephaly 53 dysbindin gene 53 SIRT1 protein 53 CFTR gene 53 JAK2 gene 53 SCA5 53 uterus didelphys 53 congenital glaucoma 53 Von Willebrand 53 leukoencephalopathy PML 53 BCL#A 53 blood clotting disorder 53 MeCP2 gene 53 parainfluenza virus 53 demyelinating 53 huntingtin gene 53 PDD NOS 53 leptin deficiency 53 hydrocephaly 53 primary ciliary dyskinesia 53 chromosomal anomalies 53 #beta HSD1 53 JAK mutations 53 HELLP 53 TCF#L# gene 53 neuro degenerative disease 53 transfusion syndrome 53 Obstructive sleep apnea 53 late infantile neuronal 53 Aortic dissection 53 sensorimotor 53 retinoblastoma 53 Inappropriate activation 53 polyhydramnios 53 apoE4 53 motor neuron 53 Tay Sachs Disease 53 paralysis blindness 53 Eosinophilic 53 #q# deletion syndrome 53 degenerative nerve 53 Stargardt disease 53 dyslexia 53 neural plasticity 53 coagulopathy 53 Irritable bowel syndrome 53 dopaminergic neurons 53 opsoclonus myoclonus syndrome 53 Celiac sprue 53 degenerative nerve disorder 53 thyroid hormone deficiency 53 debilitating neurological disorder 53 genetic abnormalities 53 misregulation 53 GPC5 53 Mitochondrial dysfunction 53 congenital scoliosis 53 AV conduction 53 polycystic ovarian syndrome PCOS 53 amyloidosis 53 susceptibility gene 53 anosognosia 53 BRAF gene 53 disorders FASD 53 optic atrophy 53 PTEN gene 53 AAT Deficiency 53 Asberger Syndrome 53 alpha synuclein gene 53 Treacher Collins Syndrome 53 neurological degeneration 53 mGluR5 antagonist 53 metabolic acidosis 53 Frontal lobe 53 anencephaly 53 behavioral disinhibition 53 brain plasticity 53 torticollis 53 incurable neurological disease 53 Maroteaux Lamy syndrome 53 prion disease 53 dystrophin gene 53 phenylketonuria 53 myasthenia gravis MG 53 Autism Spectrum Disorders ASD 53 Cystic fibrosis 53 myeloproliferative neoplasms 53 FSGS 53 Vitamin B# deficiency 53 cri du chat 53 Acute Myelogenous Leukemia 53 C EBP alpha 53 primary progressive aphasia 53 beta globin gene 53 genes predisposing 53 filaggrin 53 Parkinson disease PD 53 myelination 53 granule cells 53 Systemic lupus erythematosus SLE 53 hemiparesis 53 protein tau 53 mutation 53 eosinophilic 53 tricuspid atresia 53 neurodevelopmental impairment 53 Battens Disease 53 celebral palsy 53 progranulin gene 53 protein misfolding 53 herpesviruses 53 Fetal alcohol 53 autism cerebral palsy 53 congenital anomaly 53 supratentorial 53 chromosome rearrangements 53 prematurity ROP 53 neuronal function 53 leptin receptor 53 hyperprolactinemia 53 hyperparathyroidism 53 Gestational diabetes 53 Hip dysplasia 53 Sturge Weber 53 Ichthyosis 53 tremors slowness 53 malformation 53 HMGA2 53 MELAS syndrome 53 inappropriate antidiuretic hormone SIADH 53 Alzhiemer 53 NKX2 53 caveolin 53 hypopituitarism 53 familial hypercholesterolemia 53 MECP2 53 progranulin 53 spontaneous mutation 53 GH deficiency 53 Sudden Arrhythmia Death 53 profound deafness 53 hemolytic anemia 53 chromosomal abnormalities 53 lymphocytic 53 phenotypes 53 Wnt signaling 53 neonatal encephalopathy 53 fibrodysplasia ossificans progressiva 53 premorbid 53 Alagille syndrome 53 neural cells 53 protein dystrophin 53 osteogenic sarcoma 53 Lafora 53 obsessive compulsive behaviors 53 chronic degenerative 53 skeletal abnormalities 53 folate metabolism 53 congenital hypothyroidism 53 frontal temporal dementia 53 Systemic lupus 53 cholinergic tone 53 mild cognitive 53 primary immunodeficiency 53 mammary tumors 53 galanin 53 Marfan syndrome 53 maternally transmitted 53 dysbindin 53 glutamic acid decarboxylase 53 Polycystic ovary syndrome 53 SLC#A# [002] 53 Prox1 53 dystrophic 53 recessive inheritance 53 Ataxia Telangiectasia 53 Spinal Muscular Atrophy 53 behavioral disturbances 53 functioning autistic