Related by context. All words. (Click for frequent words.) 66 hereditary deafness 66 profound deafness 65 chromosome abnormality 64 chromosomal defect 64 recessive genetic 64 Usher Syndrome 64 auditory neuropathy 64 mitochondrial disorders 63 deafness 63 Becker muscular dystrophy 63 de novo mutations 63 neuropsychiatric disorder 62 neuro developmental disorder 62 holoprosencephaly 62 chromosomal anomaly 62 hereditary predisposition 62 neurodevelopmental disorder 62 CHARGE syndrome 62 chromosomal disorder 62 Spinal muscular atrophy 62 Usher syndrome 62 Dravet syndrome 62 sensorineural hearing loss 61 autistic regression 61 genetic abnormality 61 Rett syndrome 61 Kufs disease 61 Hurler Syndrome 61 autism spectrum disorders ASDs 61 Joubert syndrome 61 behavioral disturbances 61 enterocolitis 60 MCAD deficiency 60 polycystic ovarian syndrome PCOS 60 rare chromosomal disorder 60 Prader Willi syndrome 60 neurobehavioral disorder 60 Apert syndrome 60 neurodevelopment disorder 60 dyskeratosis congenita 60 achromatopsia 60 CHDs 60 otosclerosis 60 inherited mutations 60 hypertrophic cardiomyopathy HCM 60 hereditary disorder 60 Alport Syndrome 60 congenital blindness 60 fatal neurodegenerative disorder 60 autism neurological disorder 60 ectodermal dysplasia 60 degenerative neurological diseases 60 Krabbe Disease 60 cochlear implantation 60 debilitating neurological disorder 59 autosomal recessive disease 59 hormonal abnormalities 59 Sudden Unexplained Death 59 Coeliac disease 59 severe dehydrating diarrhea 59 brain lesions 59 skeletal dysplasia 59 varicella infection 59 retinal dysfunction 59 presbycusis 59 asperger syndrome 59 Sanfilippo Syndrome 59 Lafora disease 59 neurological disorder affecting 59 Hutchinson Gilford progeria 59 brain malformation 59 thyroid hormone deficiency 59 alpha thalassemia 59 ASDs 59 fronto temporal dementia 59 neurosensory 59 Genetic mutation 59 G6PD deficiency 59 Rotavirus infection 59 pseudotumor cerebri 59 neuro degenerative disorders 59 Dwarfism 59 Crouzon syndrome 59 HGPS 59 molar pregnancy 59 VCFS 59 congenital birth defects 59 Hurler syndrome 59 developmental abnormalities 59 biochemical imbalance 59 Genetic variants 59 idiopathic epilepsy 59 hydrops 59 MECP2 gene 59 spastic diplegia 59 congenital adrenal hyperplasia CAH 59 Iron deficiency anemia 59 ataxia telangiectasia 59 Vitamin B# deficiency 59 medulloblastoma tumors 58 fatal neuromuscular disorder 58 Severe Primary IGFD 58 degenerative neurological disorder 58 epigenetic alterations 58 congenital disorders 58 Angelman Syndrome 58 Aortic stenosis 58 dominantly inherited 58 metabolic abnormality 58 neuropsychological impairments 58 Phenylketonuria PKU 58 JAK mutations 58 recessive trait 58 immunodeficiency disorder 58 congenital hypothyroidism 58 autosomal dominant disorder 58 blastoma 58 monozygotic twin 58 spinal muscular atrophy SMA 58 genetic syndromes 58 prenatally diagnosed 58 polymorphic ventricular tachycardia 58 Irlen Syndrome 58 sporadic Creutzfeldt Jakob 58 neurological abnormalities 58 epilepsies 58 MCADD 58 immuno deficiency 58 Down syndrome cerebral palsy 58 Congenital Adrenal Hyperplasia 58 Rh incompatibility 58 degenerative neurological disease 58 Sporadic CJD 58 thyroid deficiency 58 Klinefelter syndrome 58 Genetic predisposition 58 Krabbe Leukodystrophy 58 neurocognitive dysfunction 58 autosomal dominant inheritance 58 inherited neurological disorder 58 genetically inherited 58 dysgenesis 58 Rett syndrome neurological disorder 58 Angelman syndrome 58 Hutchinson Gilford Progeria 58 fatal myelination disorder 58 prematurity ROP 58 narcolepsy cataplexy 57 disorder thalassemia 57 neonatal encephalopathy 57 mitochondrial dysfunction 57 incurable genetic 57 pyloric stenosis 57 predisposing factor 57 testicular tumors 57 type 1diabetes 57 Hirschsprung Disease 57 habitual snoring 57 Excessive daytime sleepiness 57 unprovoked seizures 57 hormonal disorder 57 Hirschsprung disease 57 Retinoblastoma 57 gastrointestinal dysfunction 57 progeria rare 57 WAGR syndrome 57 Brugada syndrome 57 disorders ASD 57 Leber congenital amaurosis LCA 57 chromosome deletion 57 spasmodic dysphonia 57 Pneumococcal pneumonia 57 Noonan Syndrome 57 galactosemia 57 leukoencephalopathy 57 irreversible blindness 57 involuntary tics 57 precocious puberty 57 otitis 57 Li Fraumeni syndrome 57 Severe Combined Immunodeficiency 57 disorder ASD 57 craniofacial abnormalities 57 commonest cause 57 myotonic dystrophy 57 chromosomal abnormality 57 leptin deficiency 57 DiGeorge Syndrome 57 congenital glaucoma 57 roseola 57 neuro degenerative disorder 57 epigenetic changes 57 Hip dysplasia 57 myelomeningocele 57 chromosomal disorders 57 Hereditary angioedema 57 hereditary spastic paraplegia 57 primary ciliary dyskinesia 57 myelogenous leukemia 57 progressive neurodegenerative 57 autosomal recessive 57 Fragile X gene 57 multisystem disease 57 epilepsy cerebral palsy 57 neurological impairments 57 Reactive Attachment Disorder 57 Hutchinson Gilford Progeria Syndrome 57 transfusion syndrome 57 Cystic fibrosis CF 57 childhood disintegrative disorder 57 embryonal rhabdomyosarcoma 57 Pompe Disease 57 neurobiological disorder 56 limb malformations 56 craniofacial defects 56 Moebius Syndrome 56 enuresis 56 Alport syndrome 56 Raynaud disease 56 neuroblastomas 56 alzheimer disease 56 Medulloblastoma 56 Moebius syndrome 56 idiopathic generalized epilepsy 56 Nephrotic Syndrome 56 polydactylism 56 Duchenne muscular dystrophy DMD 56 persistent pulmonary hypertension 56 Autistic Spectrum Disorder 56 systemic scleroderma 56 paralysis blindness 56 medium chain acyl 56 autoinflammatory diseases 56 neurological sequelae 56 undiagnosed celiac disease 56 thyroid dysfunction 56 limb deformities 56 fatal neurodegenerative 56 chromosomal imbalance 56 spastic paraplegia 56 cerebral palsy blindness 56 Myotonic dystrophy 56 encephalitis swelling 56 recurrent miscarriages 56 dysautonomia 56 gene MECP2 56 Postnatal depression 56 NF2 56 nerve degeneration 56 CHD7 56 IgA deficiency 56 Marfan Syndrome 56 mitochondrial mutations 56 rhinovirus infection 56 hyperemesis 56 dyslexia dyspraxia 56 Fragile X syndrome 56 Perthes disease 56 idiopathic pulmonary arterial hypertension 56 optic atrophy 56 histiocytosis 56 Aortic dissection 56 developmental disorder 56 progressive neurodegenerative disorder 56 shortened telomeres 56 gastroesophageal reflux GERD 56 epidermolysis bullosa EB 56 Polycystic Ovary Syndrome 56 dysphasia 56 Sexsomnia 56 autism 56 Proteus syndrome 56 mitochondrial disease 56 Guillain Barré Syndrome 56 autistic traits 56 neuro degenerative disease 56 Peanut allergy 56 recessively inherited 56 Cockayne syndrome 56 neurological dysfunction 56 Mycoplasma pneumoniae 56 Male pattern baldness 56 recurrent infections 56 enlarged adenoids 56 spontaneous miscarriages 56 autoimmune thyroiditis 56 NF1 56 MELAS 56 Crigler Najjar syndrome 56 familial hypercholesterolaemia FH 56 degenerative disorder 56 persistent genital arousal 56 idiopathic scoliosis 56 Menkes disease 56 febrile convulsions 56 autism spectrum disorders ASD 56 neuro developmental 56 Beta thalassemia 56 variable immunodeficiency 56 lymphangioleiomyomatosis LAM 56 Gestational diabetes 56 Polycystic Ovarian Syndrome PCOS 56 Chronic fatigue 56 Anencephaly 55 Meckel Gruber 55 neurodevelopmental disorders 55 motor neurone 55 Premature Ovarian Failure 55 acute lymphoid leukemia 55 maturational 55 disorder FASD 55 skeletal abnormalities 55 multisystem disorder 55 bronchopulmonary dysplasia 55 neurodegenerative disorder 55 Proteus Syndrome 55 biochemical imbalances 55 cerebellar hypoplasia 55 Excessive sweating 55 diffuse intrinsic pontine glioma 55 rheumatic disease 55 herpes simplex encephalitis 55 hypothalamic hamartoma 55 Attention Deficit Hyperactive Disorder 55 necrotising enterocolitis 55 Mitochondrial diseases 55 congenital anomaly 55 Progeria 55 ataxias 55 middle ear effusion 55 hereditary disorders 55 #q#.# deletion syndrome 55 Mental retardation 55 reproductive endocrine 55 inherited predisposition 55 phthalate syndrome 55 ARVD 55 da mage 55 maternally transmitted 55 Klinefelter Syndrome 55 aneuploidies 55 epilepsy 55 osteogenesis imperfecta 55 progressive degenerative neurological 55 neurobehavioral disorders 55 autosomal dominant 55 thrombophilia 55 incurable degenerative 55 G#S mutation 55 apraxia 55 Tay Sachs disease 55 congenital CMV 55 physiological abnormalities 55 ADA SCID 55 Reye syndrome 55 hypophosphatasia 55 AAT deficiency 55 RSV infections 55 Fatty liver 55 ichthyosis vulgaris 55 lichen planus 55 chromosomal defects 55 Intussusception 55 inherited retinal degeneration 55 vasa previa 55 Genetic mutations 55 heritable diseases 55 chlamydial infections 55 familial dysautonomia 55 bladder exstrophy 55 hyperinsulinism 55 acute psychosis 55 Obsessive compulsive disorder 55 degenerative neuromuscular disease 55 heritable genetic 55 ApoE gene 55 Pervasive Developmental Disorder 55 autism dyslexia 55 Niemann Pick disease 55 DiGeorge syndrome 55 Muscular dystrophy 55 molluscum contagiosum 55 debilitating neurodegenerative disorder 55 post natally 55 Legg Calvé Perthes disease 55 generalized epilepsy 55 Magnesium deficiency 55 syndrome FAS 55 muscle degeneration 55 mosaicism 55 idiopathic pulmonary 55 microchimerism 55 chronic granulomatous disease 55 anatomical abnormalities 55 Parkinson disease neurological disorder 55 dysphonia 55 mental retardation cerebral palsy 55 MC4R gene 55 hepatoblastoma 55 infertility miscarriages 55 familial clustering 55 Polycystic ovary syndrome PCOS 55 congential 55 nephrosis 55 microcephalin 55 Leber Congenital Amaurosis LCA 55 non syndromic 55 polycystic ovaries 55 chronic obstructive airway 55 Histiocytosis 55 NPHP 55 Crohns disease 54 Rhesus disease 54 Oppositional Defiant Disorder 54 spontaneous mutations 54 neurodevelopmental disability 54 Pervasive Developmental Disorders 54 T1DM 54 Male infertility 54 hypotonia 54 hydrocephaly 54 primitive neuroectodermal tumors 54 Dental caries 54 familial adenomatous polyposis 54 Bronchiolitis 54 congenital disorder 54 enteroviral infection 54 cerebral palsy epilepsy 54 Aspergers Syndrome 54 genetic disorder 54 renovascular hypertension 54 genetic defect 54 blood clotting disorder 54 mitochondrial diseases 54 CNTNAP2 54 infertility miscarriage 54 Asberger 54 nonhereditary 54 Fragile X Syndrome 54 neurocognitive impairment 54 muscular dystrophy cystic fibrosis 54 Treacher Collins syndrome 54 orchitis 54 myalgic encephalomyelitis ME 54 autosomal dominant polycystic kidney 54 autosomal recessive disorder 54 amyloid toxicity 54 incurable neurological disorder 54 polycystic ovary syndrome PCOS 54 Myasthenia gravis 54 chromosomal anomalies 54 neuro degenerative 54 ototoxicity 54 progressive neuromuscular 54 Cryptococcus neoformans 54 GH deficiency 54 perinatal asphyxia 54 SNHL 54 Eisenmenger syndrome 54 dyscalculia 54 systemic amyloidosis 54 Von Willebrand disease 54 septo optic dysplasia 54 developmental disorders 54 cystic kidney 54 atypical hemolytic uremic syndrome 54 diagnosed prenatally 54 genital deformities 54 Cochlear implants 54 pneumococci 54 cortical plasticity 54 induced cardiomyopathy 54 hemolytic disease 54 Crouzon Syndrome 54 swollen testicles 54 Endometrial cancer 54 mitochondrial myopathy 54 neurocysticercosis 54 cortical blindness 54 Polycystic kidney disease 54 von Hippel Lindau 54 Beckwith Wiedemann Syndrome 54 streptococcus infection 54 hereditary blindness 54 Bardet Biedl syndrome 54 carbohydrate intolerance 54 Wolf Hirschhorn 54 Acute Respiratory Failure 54 laryngospasm 54 congenital anomalies 54 biliary atresia 54 static encephalopathy 54 IUGR 54 oral thrush 54 autosomal recessive genetic 54 familial hypercholesterolemia 54 Hyperthyroidism 54 neurologic deficits 54 spastic cerebral palsy 54 Vitamin D insufficiency 54 neurocognitive deficits 54 Combined Immune Deficiency 54 amusia 54 Smith Magenis syndrome 54 myopathies 54 spongiform encephalopathies 54 petit mal seizures 54 gestational diabetes mellitus GDM 54 CALHM1 54 Tourette syndrome neurological disorder 54 MYH9 gene 54 VUR 54 aniridia 54 Essential tremor 54 astrocytomas 54 hormone imbalances 54 degenerative neurological condition 54 CDH1 54 ocular albinism 54 Churg Strauss syndrome 54 Spinal Muscular Atrophy SMA 54 primary immunodeficiencies 54 cystic fibrosis hereditary 54 Gender Identity Disorder 54 Wilms Tumour 54 BH4 deficiency 54 Wernicke Korsakoff syndrome 54 rheumatic disorders 54 Genital herpes 54 retinitis pigmentosa RP 54 PANDAS 54 Obstructive sleep apnea 54 immuno compromised individuals 54 torticollis 54 Reye syndrome rare 54 hydatid disease 54 retinal degenerative disease 54 Folic acid deficiency 54 Major depressive disorder 54 Peutz Jeghers syndrome 54 psychosocial dwarfism 54 mental retardation epilepsy 54 Heavy menstrual bleeding 54 Myocarditis 54 GBA mutations 54 Duchenne Muscular Dystrophy DMD 54 Von Hippel Lindau 54 autism Asperger Syndrome 54 lymphoblastic leukemia 54 autistic tendencies 54 DISC1 gene 54 xeroderma pigmentosum 54 immunodeficiency 54 Biliary Atresia 54 Otitis media 54 leukodystrophy 54 nongenetic 54 recurrent miscarriage 54 Lesch Nyhan syndrome 54 Viral infections 54 polycystic 54 Thyroid disorders 54 inherited neurodegenerative 53 biliary atresia rare 53 Rett Syndrome 53 Premature ejaculation 53 uncontrolled epilepsy 53 Leber Hereditary Optic Neuropathy 53 Bed wetting 53 valvular heart disease 53 familial ALS 53 dimentia 53 Sudden infant 53 Bruxism 53 disabling neurological 53 muscular degeneration 53 congenital diaphragmatic hernia 53 craniosynostosis 53 phonic tics 53 SRBD 53 amniotic fluid embolism 53 Leber congenital amaurosis 53 FXTAS 53 Autism Spectrum Disorders ASD 53 precancerous condition 53 Aicardi syndrome 53 Bacterial vaginosis 53 impaired cognition 53 neurologic disorders 53 Leber hereditary optic neuropathy 53 premenstrual syndrome PMS 53 de ath 53 umbilical hernias 53 Aplastic anemia 53 childhood leukemias 53 Wilm tumor 53 Hashimoto thyroiditis 53 congenital abnormalities 53 verbal apraxia 53 Hypophosphatasia 53 familial adenomatous polyposis FAP 53 lipodystrophy syndrome 53 autism Asperger 53 Parkinson disease neurodegenerative disorder 53 disabling neurological condition 53 Retinopathy 53 inheritable genetic 53 Cerebral malaria 53 Misdiagnosis 53 upper airway obstruction 53 acute otitis media 53 BMPR2 53 perinatally 53 chromosome abnormalities 53 motor neuron diseases 53 autism spectrum disorders 53 LQTS 53 #q# deletion syndrome 53 stem glioma 53 CMV infections 53 neuro developmental disorders 53 congenital CMV infection 53 telltale symptom 53 Autoimmune disorders 53 enzyme deficiency 53 neurodevelopment disorders 53 neurodevelopmental outcomes 53 chronic autoimmune disorder 53 diabetes insipidus 53 clefting 53 osteogenesis imperfecta OI 53 lacunar 53 craniofacial anomalies 53 acute rheumatic fever 53 leukodystrophies 53 lactase deficiency 53 Rheumatic fever 53 Down syndrome spina bifida 53 polymyalgia rheumatica 53 microvascular dysfunction 53 genital herpes infections 53 Behavior Disorder 53 hypothalamic pituitary adrenal axis 53 human papillomaviruses HPV 53 glutamate signaling 53 Hypertrophic cardiomyopathy 53 deformed limbs 53 congenital defects 53 Zinc deficiency 53 immunodeficiency diseases 53 tic disorders 53 systemic mastocytosis 53 Hemolytic Uremic Syndrome 53 reproductive tract infections 53 motor neuron degeneration 53 lupus scleroderma 53 cystic fibrosis muscular dystrophy 53 Bedwetting 53 Fanconi Anemia 53 congenital toxoplasmosis 53 respiratory viral infections 53 Asperger syndrome milder 53 adenomyosis 53 facioscapulohumeral muscular dystrophy 53 fat malabsorption 53 juvenile myelomonocytic leukemia 53 Friedreich ataxia 53 Epileptic seizures 53 atopic eczema 53 disorders FASD 53 underlying pathophysiology 53 Inflammatory Bowel 53 unexplained infertility 53 discoid lupus 53 Spina bifida 53 Angelman 53 Niemann Pick 53 immunodeficiencies 53 comorbid disorders 53 skeletal malformations 53 Holoprosencephaly 53 untreated celiac disease 53 microvascular angina 53 anencephaly 53 cleft lip palate 53 Sandhoff disease 53 atypical parkinsonism 53 meningitis encephalitis 53 Chromosomal abnormalities 53 Glioblastoma Multiforme GBM 53 dementing 53 corneal dystrophy 53 febrile convulsion 53 syndrome OSAS 53 Reye Syndrome 53 Stargardt Macular Dystrophy 53 type2 diabetes 53 Synovial Sarcoma 53 Mitochondrial disease 53 osteopetrosis 53 #q# deletion 53 developmental delays 53 post partum psychosis 53 nondemented 53 deafness blindness 53 primary ovarian insufficiency 53 renal scarring 53 Morquio syndrome 53 paraneoplastic 53 degenerative nerve disorder 53 recessive genes 53 Guillain Barre Syndrome GBS 53 HbF 53 progressive multifocal PML 53 haemolytic anemia 53 Wilms tumors 53 aetiological 53 Mild cognitive impairment 53 enterovirus infection 53 juvenile idiopathic arthritis JIA 53 placenta praevia 53 alpha1 antitrypsin deficiency 53 diabetic retinopathy DR 53 vitamin B1 deficiency 53 threatening peanut allergies 53 spinal bifida 53 Langerhans cell histiocytosis 53 Premature birth 53 Pulmonary fibrosis 53 ventricular cardiomyopathy 53 MYCN amplification 53 neurobiological disorders 53 hypogonadotropic hypogonadism 53 amnestic 53 PPCM 53 selective mutism 52 invasive Hib 52 Hyperactivity 52 Fetal alcohol 52 Urinary tract infections 52 pulmonary hypertension PH 52 utero exposure 52 PIDD 52 neuromuscular disorder 52 polyhydramnios 52 ADPKD 52 MeCP2 gene 52 polycystic ovary syndrome 52 spinal muscle atrophy 52 Lennox Gastaut syndrome 52 necrotizing enterocolitis NEC 52 lysosomal storage diseases 52 polycystic kidneys 52 Motor neurone disease 52 craniofacial deformities 52 Ménière disease 52 Raynaud syndrome 52 neurodevelopmental impairment 52 Autistic Spectrum Disorders 52 cardio myopathy 52 Alzheimers disease 52 dysfunctioning 52 recurrent seizures 52 malignant myeloma 52 aortic rupture 52 Acute pancreatitis 52 genes predisposing 52 juvenile idiopathic arthritis 52 spinocerebellar ataxia 52 cerebral hypoxia 52 bacterium Neisseria meningitidis 52 genomic variants 52 mito 52 cardiac arrythmia 52 savant syndrome 52 inappropriate antidiuretic hormone SIADH 52 glucocorticoid receptors 52 idiopathic PAH 52 meningitis septicemia 52 fibroids endometriosis 52 Joubert syndromes 52 vascular birthmarks 52 genomic imprinting 52 related maculopathy 52 imperfecta 52 Sjögren syndrome 52 monogenic 52 filaggrin 52 Atopic dermatitis 52 Hydrocephalus 52 disease CJD 52 Dravet 52 TEL AML1 52 congenital abnormality 52 Beckwith Wiedemann syndrome 52 Neurological disorders 52 Down syndrome chromosomal disorder 52 epididymitis 52 cortical dysplasia 52 postnatally 52 1 Antitrypsin Deficiency 52 Cleft palate 52 diffuse pontine glioma 52 germline mutations 52 mental retardation blindness 52 Overactive bladder 52 gene APOE4 52 complex neurobiological disorder 52 hyperprolactinemia 52 Epstein Barr virus EBV 52 Chiari malformation 52 male reproductive tract 52 eczema hay fever 52 lethargy irritability 52 herpes infection 52 swallowing reflex 52 pneumococcal infection 52 Neurofibromatosis Type 52 neurogenerative diseases 52 SHANK3 52 abnormal genital 52 Folate deficiency 52 urethritis 52 Pre eclampsia 52 Diamond Blackfan anemia 52 BRIP1 52 pulmonary thromboembolism 52 GAB2 52 Primary IGFD 52 chronic neurological disorder 52 cerebellar ataxia 52 lethal arrhythmias 52 Osteogenesis imperfecta 52 tricuspid atresia 52 fibromatosis 52 muscular dystrophy sufferers 52 Duchene muscular dystrophy 52 vesicoureteral reflux VUR 52 ORMDL3 52 PCOD 52 enlarged tonsils 52 lissencephaly 52 twin transfusion 52 progranulin mutations 52 lysosomal storage disorder 52 Porphyria 52 Childhood Disorder 52 premenstrual dysphoric disorder PMDD 52 infantile hemangioma 52 anatomic abnormalities 52 Tourette Syndrome neurological disorder 52 bicuspid valve 52 Hoarseness 52 Acute myeloid leukemia 52 genetic disorders 52 neurologic disorder 52 reproductive abnormalities 52 acute myeloid 52 epigenetic modification 52 unexplained fainting 52 Lactose intolerance 52 Duchene Muscular Dystrophy 52 mastocytosis 52 status epilepticus 52 placental malaria 52 bicuspid aortic valves 52 lysosomal diseases 52 lysosomal storage disease 52 neurological disorder characterized 52 motor neuropathy 52 Tay Sachs Disease 52 immunopathology 52 Irritable bowel syndrome 52 Arteriovenous Malformation 52 neurologic sequelae 52 spontaneous remission 52 malignant brain 52 Canavan Disease 52 Tourette Syndrome TS 52 consanguineous marriages 52 olfactory dysfunction 52 peripartum cardiomyopathy 52 pulmonary hypoplasia 52 Peritoneal mesothelioma 52 untreated sleep apnea 52 intractable epilepsy 52 gender dysphoria 52 fetal malformations 52 mtDNA mutations 52 Chronic pancreatitis 52 HIBM 52 neurological degeneration 52 underactive thyroid gland 52 facial clefts 52 untreated ADHD 52 LRRK2 mutations 52 NOMID 52 pneumonia septicemia 52 myasthenia gravis neuromuscular 52 Diabetic neuropathy 52 Fanconi Anaemia 52 ovarian dysfunction 52 degenerative muscular 52 sonographic diagnosis 52 chorioamnionitis 52 MEF2A 52 chlamydial infection 52 quadriplegic cerebral palsy 52 respiratory gastrointestinal 52 ANCA associated 52 Loeys Dietz syndrome 52 Fanconi anemia rare 52 cerebral palsy autism 52 Polycystic ovarian syndrome 52 deafness neurological 52 cytomegalovirus infection 52 Ankylosing spondylitis 52 hamartoma 52 MODY 52 metachromatic leukodystrophy 52 underactive thyroids 52 undiagnosed untreated 52 Periodontal disease 52 Hereditary angioedema HAE 52 missense mutations 52 Autism Spectrum Disorders ASDs 52 neuroblastoma tumor 52 antenatal screening 52 antenatal depression 52 atresia 52 meningoencephalitis 52 BCL#A 52 microencephaly 52 LC#m# vaccine 52 PNET 52 Sjogren Syndrome 52 Infantile spasms 52 Celiac sprue 52 aspergers 52 Down syndrome 52 otitis media 52 keloid scars 52 clotting disorder 52 inconsolable crying 52 peripartum 52 auditory verbal 52 recurrent abdominal pain 52 biological predisposition 52 lateral sclerosis ALS 52 Retinitis Pigmentosa RP 52 huntingtin gene 52 euthymic patients 52 Guillain Barré 52 manic depressive disorder 52 nonsense mutation 52 neuronal dysfunction 52 thoracic aortic disease 52 Craig Shergold 52 chiari malformation 52 PCNSL 52 Chronic insomnia 52 debilitating affliction 52 Gorlin syndrome 52 neurofibromatosis genetic disorder 52 Sensorineural hearing loss 52 juvenile myoclonic epilepsy 52 achondroplasia 52 subarachnoid haemorrhage 52 choriocarcinoma 52 malarial infection 52 behavioral abnormalities 51 neurodermatitis 51 kernicterus 51 inherited genetic mutation 51 blindness paralysis 51 benign positional vertigo 51 spontaneous mutation 51 Neisseria meningitides 51 proband 51 Levy Lahad 51 autism Asperger syndrome 51 Nasal allergies 51 muscular dystrophies 51 HELLP 51 Prion diseases 51 Meningiomas 51 Waldenstrom macroglobulinemia 51 MECP2 51 Krabbe leukodystrophy 51 Polycystic Ovary Syndrome PCOS 51 generalized seizures 51 genetic abnormalities 51 puerperal psychosis 51 EBV infection 51 Febrile seizures 51 medulloblastomas 51 nonalcoholic cirrhosis 51 cerebral palsy Down syndrome 51 haemochromatosis