Related by context. All words. (Click for frequent words.) 63 neuro developmental disorder 63 CHARGE syndrome 62 Noonan Syndrome 62 neurodevelopment disorder 62 chromosomal disorder 62 Polycystic kidney disease 61 neuro developmental 61 degenerative disorder 61 spastic diplegia 61 progressive neurodegenerative disorder 61 autism neurological disorder 60 Alport Syndrome 60 Crouzon Syndrome 60 mental retardation cerebral palsy 60 dominantly inherited 59 Becker muscular dystrophy 59 neuropsychiatric disorder 59 Zinc deficiency 59 cystic fibrosis hereditary 59 undiagnosed celiac disease 59 Ehlers Danlos syndrome 59 Joubert Syndrome 59 Congenital heart 59 Mitochondrial disease 59 neurobiological disorder 59 Myotonic dystrophy 59 chromosomal defect 59 Treacher Collins syndrome 59 neurodevelopmental disorder 59 Rubinstein Taybi syndrome 59 Proteus syndrome 58 septo optic dysplasia 58 Krabbe leukodystrophy 58 neurofibromatosis NF 58 chromosome abnormality 58 neurogenetic 58 Iron deficiency 58 rare chromosomal disorder 58 neurobehavioral disorder 58 cystic fibrosis muscular dystrophy 58 congenital diaphragmatic hernia 58 Biliary atresia 58 Crouzon syndrome 58 Krabbe Disease 58 retinal dysfunction 58 Tay Sachs disease 58 chiari malformation 58 incurable neurological disorder 58 Polycystic ovary syndrome PCOS 58 Spinal muscular atrophy 58 Premature birth 58 Joubert syndrome 58 recessive genetic 58 static encephalopathy 58 Usher Syndrome 58 hydrops 57 Arnold Chiari Malformation 57 osteogenesis imperfecta 57 Spina bifida 57 Rh incompatibility 57 optic nerve hypoplasia 57 Von Willebrand disease 57 neurological disorder affecting 57 DiGeorge syndrome rare 57 incurable neurodegenerative disease 57 neurofibromatosis genetic disorder 57 Muscular dystrophy 57 inherited neurological disorder 57 Alagille syndrome 57 Tourette syndrome neurological disorder 57 degenerative neuromuscular disease 57 Dravet syndrome 57 neurodegenerative disorder characterized 57 holoprosencephaly 57 DiGeorge syndrome 57 mental retardation blindness 57 Osteogenesis imperfecta 56 inherited neurodegenerative 56 Tuberous sclerosis 56 thyroid hormone deficiency 56 Sanfilippo Syndrome 56 psychosocial dwarfism 56 skeletal dysplasia 56 VCFS 56 myelogenous leukemia 56 congenital CMV 56 debilitating neurological disorder 56 Morquio syndrome 56 mitochondrial myopathy 56 childhood disintegrative disorder 56 medium chain acyl 56 Genetic predisposition 56 Birth defects 56 neurodevelopmental disability 56 Celiac sprue 56 osteosarcoma bone 56 Krabbe Leukodystrophy 56 ocular albinism 56 Cerebral palsy 56 congenital disorders 56 neural tube defect 56 Autoimmune disorders 56 juvenile myelomonocytic leukemia 56 dystonia neurological movement 56 immunodeficiency disorder 56 bronchopulmonary dysplasia 56 Sudden infant 56 hereditary degenerative 56 Hurler syndrome 56 Erb palsy 56 hormonal disorder 56 Beta thalassemia 56 molar pregnancy 56 Magnesium deficiency 56 retinitis pigmentosa degenerative 56 spinal bifida 56 Fetal alcohol 56 inherited mutations 56 Niemann Pick 56 prematurity ROP 56 genetic abnormality 56 brain malformation 55 autism spectrum disorders ASDs 55 Sturge Weber syndrome 55 Canavan Disease 55 juvenile dermatomyositis 55 gastroschisis 55 progressive neurodegenerative 55 cerebral palsy epilepsy 55 limb malformations 55 congenital disorder 55 muscular dystrophy cystic fibrosis 55 Mitochondrial diseases 55 ectodermal dysplasia 55 Polycystic ovarian syndrome 55 Beckwith Wiedemann Syndrome 55 Medulloblastoma 55 congenital glaucoma 55 mitochondrial disease 55 Klinefelter syndrome 55 fibrodysplasia ossificans progressiva FOP 55 hereditary disorder 55 seizures comas 55 velo cardio facial 55 Major depressive disorder 55 Apert syndrome 55 biliary atresia rare 55 Obstetric fistula 55 Infant botulism 55 nonalcoholic cirrhosis 55 degenerative neurological disease 55 CHDs 55 Cockayne syndrome 55 verbal apraxia 55 Hutchinson Gilford progeria 55 insulin resistance syndrome 55 genetic disorder 55 toxemia 55 Angelman Syndrome 55 #q#.# deletion syndrome 55 HELLP 55 autosomal dominant polycystic kidney 55 Hypertrophic cardiomyopathy 55 fatal neurodegenerative disorder 55 muscular degeneration 55 Prader Willi syndrome 55 PKU genetic 55 Anencephaly 55 chromosomal anomaly 55 achondroplasia 55 Irritable bowel syndrome IBS 55 HELLP syndrome 55 Parkinson degenerative 55 Henoch purpura 55 perinatal asphyxia 55 neurodegenerative disorder 55 Atopic dermatitis 55 transfusion syndrome 55 Niemann Pick disease 55 gastrointestinal dysfunction 55 Lactose intolerance 55 Postpartum depression 55 Sporadic CJD 55 thyroid dysfunction 55 prenatally diagnosed 55 Von Hippel Lindau 55 Rhabdomyosarcoma rare 55 celiac sprue disease 55 congenital toxoplasmosis 55 Endometrial cancer 54 Cystic fibrosis CF 54 hereditary deafness 54 Acute lymphocytic leukemia 54 Severe Combined Immunodeficiency 54 blastoma 54 cystic fibrosis Duchenne muscular 54 Hip dysplasia 54 Reactive Attachment Disorder 54 myelomeningocele 54 developmental abnormalities 54 Bacterial vaginosis 54 progressive neurological disorder 54 Iron deficiency anemia 54 Difficulty swallowing 54 Li Fraumeni syndrome 54 puerperal psychosis 54 Folic acid deficiency 54 Lafora disease 54 unexplained mental retardation 54 Coeliac disease 54 neurofibromatosis 54 cerebellar ataxia 54 quadriplegic cerebral palsy 54 cystic fibrosis sickle cell 54 Arnold Chiari 54 osteogenesis imperfecta OI 54 MCADD 54 Pervasive Developmental Disorders 54 anencephaly 54 diffuse intrinsic pontine glioma 54 Parkinson disease degenerative 54 congenital birth defects 54 Kufs disease 54 osteopetrosis 54 MCAD deficiency 54 gestational diabetes mellitus GDM 54 Dilated cardiomyopathy 54 meningitis sepsis 54 serotonin imbalance 54 Lennox Gastaut Syndrome 54 inflammatory demyelinating 54 embryonal rhabdomyosarcoma 54 Genetic mutation 54 pyloric stenosis 54 hemophagocytic lymphohistiocytosis 54 chronic neurological disorder 54 Polycystic Ovarian Syndrome PCOS 54 DiGeorge Syndrome 54 Leber Congenital Amaurosis LCA 54 muscular dystrophy cerebral palsy 54 Retinoblastoma 54 Lumbar spinal stenosis 54 CdLS 54 medulloblastoma tumors 54 Peritoneal mesothelioma 54 Ewing sarcoma bone 54 Hypoplastic Left Heart 54 de novo mutations 54 Hurler Syndrome 54 progressive neurodegenerative disease 54 chromosomal abnormality 54 Osteogenesis Imperfecta 54 Childhood Disorder 54 debilitating neurological disease 54 Nonalcoholic fatty liver 54 amniotic fluid embolism 54 spastic cerebral palsy 54 autism dyslexia 54 hereditary predisposition 54 chromosomal disorders 54 petit mal seizures 54 hypoxic ischemic encephalopathy 54 degenerative retinal disease 54 Patau syndrome 54 Hirschsprung disease 54 pseudotumor cerebri 54 hereditary spastic paraplegia 54 Premature Ovarian Failure 54 epilepsy neurological disorder 54 inherited genetic mutations 54 Rett syndrome neurological disorder 54 Beckwith Wiedemann syndrome 54 diaphragmatic hernia 54 Angelman syndrome 54 dysautonomia 54 chronic autoimmune disorder 54 infertility miscarriage 54 Usher syndrome 54 spastic paraplegia 54 Pulmonary hypertension 54 fatal neuromuscular disorder 54 Leber hereditary optic neuropathy 54 chromosome #q#.# deletion 54 progeria rare 53 Foetal alcohol 53 progressive degenerative neurological 53 degenerative neurological disorder 53 autosomal recessive genetic 53 oral clefts 53 Severe Primary IGFD 53 hypotonia 53 infantile hemangioma 53 Degenerative disc disease 53 Angelman 53 anencephaly fatal 53 WAGR syndrome 53 congenital adrenal hyperplasia CAH 53 autosomal recessive disorder 53 Motor neurone disease 53 neuro muscular disorder 53 Postnatal depression 53 dysthymic disorder 53 Colorectal cancer CRC 53 Krabbe disease 53 hemolytic disease 53 Neural tube 53 Spasmodic dysphonia 53 Pelizaeus Merzbacher disease 53 Aplastic anemia 53 Pre eclampsia 53 myalgic encephalomyelitis ME 53 cystic fibrosis chronic pancreatitis 53 incurable genetic 53 idiopathic cardiomyopathy 53 developmental delays 53 AAT Deficiency 53 Hemolytic Uremic Syndrome 53 Proteus Syndrome 53 common neurovascular complication 53 lissencephaly 53 galactosemia 53 Selenium deficiency 53 enterocolitis 53 metabolic abnormality 53 Hemolytic uremic syndrome 53 Fragile X syndrome 53 Hutchinson Gilford Progeria 53 Aicardi syndrome 53 myasthenia gravis neuromuscular 53 premature birth 53 Fanconi anemia 53 degenerative muscular 53 Cognitive dysfunction 53 spinal muscular atrophy SMA 53 Chiari malformation 53 autoimmune thyroid 53 immuno deficiency 53 Alport syndrome 53 Preterm babies 53 mental retardation epilepsy 53 Malignant mesothelioma 53 CNTNAP2 gene 53 Listeria infections 53 multi infarct dementia 53 AAT deficiency 53 autosomal dominant inheritance 53 chronic granulomatous disease 53 genetic syndromes 53 Gestational diabetes 53 Fanconi Anemia 53 Eloysa Vasquez 53 fetal malformations 53 Vitamin D insufficiency 53 aniridia 53 Maternal obesity 53 Neural tube defects 53 Trisomy 53 Diamond Blackfan anemia 53 Essential tremor 53 nonhereditary 53 leukodystrophy 53 fatal neurodegenerative 53 Wilm tumor 53 primary ciliary dyskinesia 53 schizo affective disorder 53 irreversible blindness 53 unprovoked seizures 53 hypertrophic cardiomyopathy HCM 53 Rheumatic fever 53 Hemorrhagic stroke 53 Pervasive Developmental Disorder 53 cerebral palsy blindness 53 HELLP Syndrome 53 polycystic ovarian syndrome 52 debilitating neurodegenerative disorder 52 Tuberous Sclerosis Complex 52 Sturge Weber Syndrome 52 syndrome FAS 52 lymphangioleiomyomatosis LAM 52 histiocytosis 52 coma convulsions 52 retinal degenerative disease 52 Uveal melanoma 52 cystic kidney 52 mental retardation 52 blindness deafness 52 autoimmune thyroiditis 52 facial clefts 52 degenerative nerve disorder 52 spastic quadriplegic cerebral palsy 52 Secondhand smoke exposure 52 Preterm births 52 Shwachman Diamond Syndrome 52 hormonal abnormalities 52 Diabetic neuropathy 52 Crigler Najjar syndrome 52 aspergers syndrome 52 Aortic stenosis 52 hyperemesis gravidarum 52 ARVD 52 neonatal encephalopathy 52 apraxia 52 oligodendrogliomas 52 cerebal palsy 52 Genetic variants 52 Wilms tumor 52 respiratory insufficiency 52 Diffuse Intrinsic Pontine Glioma 52 chromosomal imbalance 52 proximal femoral focal 52 fatal myelination disorder 52 abnormal genital 52 Neurological disorders 52 genetically inherited 52 persistent pulmonary hypertension 52 congenital deafness 52 Chronic constipation 52 cerebral palsy 52 Cognitive impairment 52 respiratory gastrointestinal 52 autistic tendencies 52 truncus arteriosus 52 Pleural mesothelioma 52 Post partum depression 52 spina bifida 52 congenital anomalies 52 Apert 52 neurological sequelae 52 progressive neuromuscular 52 multisystem disorder 52 microencephaly 52 autosomal recessive disease 52 brachial plexus palsy 52 genital defects 52 neurodevelopmental disorder characterized 52 Tourette Syndrome neurological disorder 52 neural tube defects NTDs 52 Dysplasia 52 polycystic ovarian disease 52 PIDD 52 multiorgan 52 systemic scleroderma 52 multisystem disease 52 dysmotility 52 Asperger syndrome milder 52 cause cardiac channelopathies 52 Chiari Malformation 52 Aspergers Syndrome 52 Dental caries 52 Maroteaux Lamy Syndrome 52 immunodeficiencies 52 Tay Sachs thalassemia 52 Goldenhar syndrome 52 limb girdle muscular dystrophy 52 Polycystic Kidney Disease 52 Down syndrome 52 pituitary adenoma 52 intraventricular hemorrhage 52 congenital hydrocephalus 52 Chronic lymphocytic leukemia 52 Peanut allergies 52 Down syndrome spina bifida 52 syndrome chromosomal defect 52 Gluten intolerance 52 adrenoleukodystrophy ALD 52 Neurofibromatosis type 52 leptin deficiency 52 Congenital Adrenal Hyperplasia 52 cardiomyopathy weakening 52 inherited retinal degeneration 52 Acute myeloid leukemia 52 leukodystrophies 52 cerebral palsy spina bifida 52 ceroid lipofuscinosis NCL 52 mitochondrial disorders 52 hyperemesis 52 autosomal dominant disorder 52 paralysis blindness 52 Genetic mutations 52 alveolar rhabdomyosarcoma 52 discoid lupus 52 craniofacial abnormalities 52 Systemic lupus 52 sporadic Creutzfeldt Jakob 52 polycystic kidney disease 52 Korsakoff syndrome 52 dyskeratosis congenita 52 haemolytic uraemic syndrome 52 persistent genital arousal 52 Asperger Syndrome mild 52 thyroid deficiency 52 genetic defect 52 severe dehydrating diarrhea 52 Arthrogryposis 52 invasive secretory carcinoma 52 Autism Spectrum Disorders ASD 52 epidermolysis bullosa EB 51 Body dysmorphic disorder 51 lysosomal storage diseases 51 achromatopsia 51 metachromatic leukodystrophy 51 Arrhythmogenic Right Ventricular Cardiomyopathy 51 macular disease 51 spinal muscle atrophy 51 reflex sympathetic dystrophy 51 encephalitis swelling 51 neurological degeneration 51 arthrogryposis 51 Diamond Blackfan Anemia 51 infertility miscarriages 51 cerebral vascular disease 51 complex neurobiological disorder 51 smoldering myeloma 51 disorders FASD 51 congenital abnormality 51 Duchene muscular dystrophy 51 neurological ailment 51 mitochondrial defects 51 McCune Albright 51 internalizing disorders 51 autism cerebral palsy 51 tricuspid atresia 51 monogenic 51 aneuploidies 51 von Hippel Lindau 51 congenital abnormalities 51 pAkt 51 Treacher Collins 51 Carcinoid tumors 51 Marfan Syndrome 51 developmental disorder 51 Epidermolysis bullosa 51 borderline mental retardation 51 frontal temporal dementia 51 plexiform 51 hypertrophic cardiomyopathy genetic 51 developmental disorders 51 sacral agenesis 51 untreated celiac disease 51 ataxia telangiectasia AT 51 opsoclonus myoclonus syndrome 51 Alzheimers disease 51 dimentia 51 Macular degeneration 51 hereditary nonpolyposis colorectal cancer 51 tics involuntary 51 DIPG 51 polyhydramnios 51 Parkinson disease neurodegenerative disorder 51 fronto temporal dementia 51 eosinophilic esophagitis 51 Mental retardation 51 IUGR 51 Compulsive hoarding 51 Hashimoto thyroiditis 51 degenerative neurological condition 51 painful genital sores 51 Pulmonary fibrosis 51 Parkinson disease degenerative neurological 51 HIBM 51 muscular skeletal disorders 51 Bronchiolitis 51 Ohtahara syndrome rare 51 Porphyria 51 multiple sclerosis lupus 51 Prematurity 51 impaired cognition 51 Meckel Gruber 51 Hereditary angioedema HAE 51 phthalate syndrome 51 congential 51 pulmonary atresia 51 Inflammatory bowel disease 51 hormone imbalances 51 deafness neurological 51 narcolepsy cataplexy 51 Dwarfism 51 Generalized anxiety disorder 51 primary lateral sclerosis 51 optic atrophy 51 antenatal depression 51 multisystemic 51 ASD autism spectrum 51 SHANK3 gene 51 Dravet Syndrome 51 Unhealthy habits 51 Fibrous Dysplasia 51 Eclampsia 51 congenital muscular dystrophy 51 Nephrogenic Systemic Fibrosis NSF 51 Preterm birth 51 spinocerebellar ataxia 51 muscle degeneration 51 Fragile X Syndrome 51 Fatty liver 51 Friedrich Ataxia 51 bicuspid valve 51 chromosome deletion 51 eczema hay fever 51 Pneumococcal meningitis 51 Smith Lemli Opitz syndrome 51 Cardiac hypertrophy 51 Von Willebrand 51 neurodevelopmental disorders 51 roseola 51 Thyroid disorders 51 cerebral palsy autism 51 Xeroderma Pigmentosum XP 51 generalized epilepsy 51 Goldenhar Syndrome 51 Wiskott Aldrich Syndrome 51 prevent neural tube 51 CHD7 51 muscle hypertrophy 51 Treacher Collins Syndrome 51 Cleft lip 51 gene MECP2 51 Retinopathy 51 Hypertensive heart 51 Cryptococcus neoformans 51 Leber congenital amaurosis LCA 51 Antisocial personality 51 oral cleft 51 chronic degenerative 51 skeletal deformities 51 Lesch Nyhan syndrome 51 Rotavirus infection 51 RSV infections 51 placental abruption 51 Interstitial cystitis 51 lymphoblastic lymphoma 51 cleft lip cleft palate 51 Brugada Syndrome 51 Systemic lupus erythematosus SLE 51 Adrenoleukodystrophy 51 Hereditary angioedema 51 cyclic vomiting syndrome 51 chronic paranoid schizophrenia 51 Moyamoya 51 Combined Immune Deficiency 51 Myasthenia gravis 51 Klippel Trenaunay Weber 51 autism 51 ataxia telangiectasia 51 diabetes insipidus 51 Idiopathic pulmonary fibrosis IPF 51 metabolic disorder 51 TTTS 51 hydrocephaly 51 nerve degeneration 51 congenital heart 51 lymphocytic leukemia 51 Postpartum psychosis 51 cardiovascular restenosis cancer 51 profound deafness 51 Hypophosphatasia 51 chorioamnionitis 51 inherited neurodegenerative disorder 51 severely autistic nonverbal 51 cortical dysplasia 51 neurological impairments 50 cerebral palsy mental retardation 50 neurological disorder 50 congenital hyperinsulinism 50 MYH9 gene 50 Male infertility 50 Biliary Atresia 50 spina bifida defect 50 Obstructive sleep apnea OSA 50 blindness paralysis 50 retinitis pigmentosa hereditary 50 recessive dystrophic epidermolysis bullosa 50 lymphoblastic leukemia 50 neurogenic bladder 50 anoxic brain injury 50 Osteoarthritis OA 50 Depressive disorders 50 genetic imprinting 50 rheumatic disease 50 Alopecia Areata 50 biochemical imbalance 50 inappropriate antidiuretic hormone SIADH 50 recessive trait 50 Leber congenital amaurosis 50 Viral hepatitis 50 Basal cell carcinoma 50 Foetal Alcohol Spectrum Disorder 50 idiopathic pulmonary arterial hypertension 50 collagen vascular 50 lactase deficiency 50 elevated serum ALT 50 neuro degenerative disorder 50 progressive retinal degenerative 50 spina bifida cerebral palsy 50 Diabetic Ketoacidosis 50 Vitamin B# deficiency 50 Atopic eczema 50 biliary atresia 50 Ehlers Danlos Syndrome 50 orofacial clefts 50 cerebral palsey 50 nephritis 50 Retinitis pigmentosa 50 spine curvature 50 systemic amyloidosis 50 Kifuji diagnosed 50 clinically heterogeneous 50 Ankylosing spondylitis 50 Osteosarcoma 50 multiforme 50 pulmonary fibrosis lung 50 Chronic myeloid leukemia CML 50 Obstructive sleep apnea 50 esophageal atresia 50 neurodevelopmental impairment 50 acute psychosis 50 vascular birthmarks 50 chromosome #q#.# [001] 50 Febrile seizures 50 subdural bleeding 50 Apert Syndrome 50 Wilm Tumor 50 mitochondrial mutations 50 Pompe Disease 50 miscarriages stillbirths 50 Tourette Syndrome TS 50 deficiency anemia 50 congenital cataracts 50 Comorbid 50 endocrine dysfunction 50 paraneoplastic 50 alzheimer disease 50 genital abnormalities 50 Idiopathic pulmonary fibrosis 50 bloody diarrhea dehydration 50 neurodevelopment 50 polycystic ovarian syndrome PCOS 50 allergic eczema 50 nasal pharyngeal cancer 50 Recurrent miscarriage 50 chronic degenerative neurological 50 Langerhans Cell Histiocytosis 50 chronic obstructive airway 50 extreme prematurity 50 heritable genetic 50 PCNSL 50 Gastroparesis 50 congenital scoliosis 50 neurogenetic disorders 50 recurrent abdominal pain 50 Moebius syndrome 50 Heavy menstrual bleeding 50 Anorexia nervosa 50 disorder thalassemia 50 Acromegaly 50 imperfecta 50 neurocysticercosis 50 neuromotor 50 fibrous dysplasia 50 Lou Gherig Disease 50 commonest cause 50 chromosomal defects 50 preterm deliveries 50 Cystic fibrosis 50 twin transfusion 50 Hoarseness 50 Parkinson disease neurological disorder 50 post transplant lymphoproliferative 50 inherited metabolic disorders 50 familial adenomatous polyposis FAP 50 Low birthweight 50 Male pattern baldness 50 Hemolytic Uremic Syndrome HUS 50 uterine tumors 50 chronic progressive neurodegenerative 50 takes ethosuximide 50 cerebral palsy Down syndrome 50 Genital herpes 50 inherited retinal 50 Idiopathic Thrombocytopenic Purpura 50 Aicardi Syndrome 50 neural tube birth defects 50 arthrogryposis multiplex congenita 50 Peanut allergy 50 epilepsy cerebral palsy 50 aortic rupture 50 Tay Sachs Disease 50 muscular dystrophy multiple sclerosis 50 aciduria 50 Syringomyelia 50 Acute lymphoblastic leukemia 50 Ovary removal 50 Pompe disease rare 50 primary ovarian insufficiency 50 oxygen depravation 50 variable immunodeficiency 50 severely impairs 50 reproductive abnormalities 50 Non Hodgkins lymphoma 50 idiopathic PAH 50 Rotavirus infections 50 ADPKD 50 Tay Sachs genetic 50 post partum psychosis 50 Chronic pancreatitis 50 Urinary tract infection 50 Morquio Syndrome 50 Ewings Sarcoma 50 neurofibromatosis type 50 often reversible neuropsychiatric 50 Hypothyroidism 50 Sanfilippo syndrome 50 recessively inherited 50 hypertrophic obstructive cardiomyopathy 50 autosomal recessive 50 polycystic ovary syndrome PCOS 50 endocrine diseases 50 idiopathic epilepsy 50 combined immunodeficiency SCID 50 classic autism Asperger 50 chronic sinus infections 50 gynecologic malignancy 50 Urinary tract 50 biopsied embryos 50 dysgraphia 50 chronic rheumatic 50 dysgenesis 50 Moebius Syndrome 50 Attention Deficit Hyperactive Disorder 50 proliferative retinopathy 50 Myocardial infarction 50 JAK mutations 49 ataxias 49 microchimerism 49 otosclerosis 49 common disabling neurological 49 MECP2 gene 49 Joubert syndromes 49 Pulmonary arterial hypertension 49 Prostrate cancer 49 vasa previa 49 dermatomyositis 49 autoinflammatory 49 Ulcerative colitis 49 postpartum haemorrhage 49 Eisenmenger syndrome 49 neurodevelopmental 49 chromosomal alterations 49 enzyme deficiency 49 histrionic personality 49 neurofibromas 49 thyroiditis 49 congenital blindness 49 bone deformities 49 obliterative bronchiolitis 49 spina bifada 49 Leber Congenital Amaurosis 49 Amyotrophic lateral sclerosis 49 Tourette syndrome TS 49 Wet macular degeneration 49 Cockayne Syndrome 49 hereditary disorders 49 mild mental retardation 49 West Nile neuroinvasive 49 Morbid obesity 49 spectrum disorders ASD 49 Neurofibromatosis 49 enzyme lactase 49 asthmas 49 Smith Lemli Opitz 49 Barrett esophagus precancerous 49 IVF pregnancies 49 Untreated depression 49 Irritable bowel syndrome 49 disorder FASD 49 Colon polyps 49 Amyotrophic lateral sclerosis ALS 49 Muscular dystrophies 49 chromosomal abnormalities 49 stem glioma 49 malformation 49 severe obstructive pulmonary 49 clotting disorder 49 Cleft palate 49 Glioblastoma multiforme GBM 49 G6PD deficiency 49 postpartum mood 49 skeletal abnormalities 49 cerebral thrombosis 49 glycogen storage 49 Autism Spectrum Disorder ASD 49 testicular tumors 49 pulmonary hypoplasia 49 apolipoprotein E4 49 chromosome abnormalities 49 HNPCC 49 neurofibroma 49 Cancer cachexia 49 familial dysautonomia 49 disabling neurological 49 nongenetic 49 Myopathy 49 lichen planus 49 hemochromatosis 49 spastic quadriplegia 49 Wolf Hirschhorn 49 reactive attachment 49 homocystinuria 49 Myelodysplastic syndrome 49 Meniere Disease 49 hemolytic anemia 49 Oesophageal cancer 49 Schwannoma tumor 49 Churg Strauss syndrome 49 pneumonia sepsis 49 Perthes disease 49 Pericarditis 49 Cerebral palsy involves 49 bronchopulmonary dysplasia BPD 49 Polycystic ovary syndrome 49 thoracic aortic disease 49 birth defects mental retardation 49 tuberous sclerosis 49 neuro degenerative disorders 49 Rhabdomyosarcoma 49 tic disorders 49 Diabetic retinopathy 49 irregular menstruation 49 torticollis 49 mild retardation 49 Sjogren Syndrome 49 reactive hypoglycemia 49 congenital adrenal hyperplasia 49 Bulimia nervosa 49 Hormonal imbalances 49 1 diabetes T1D 49 Frontotemporal dementia 49 inoperable malignant tumor 49 Attention Deficit Disorder ADD 49 blood clotting disorder 49 Fanconi anemia rare 49 Langerhans cell histiocytosis 49 choriocarcinoma 49 postpartum hemorrhage 49 mesothelioma asbestosis 49 Psoriatic arthritis 49 Preterm delivery 49 CHD CVD 49 Duchene Muscular Dystrophy 49 pontine glioma 49 Polycythemia vera 49 uterus didelphys 49 male hormone androgen 49 neuroblastomas 49 congenital hypothyroidism 49 fatal neuromuscular 49 associated tremor ataxia 49 medulloblastoma malignant brain tumor 49 Colorectal cancers 49 Chronic Inflammatory Demyelinating Polyneuropathy 49 Knee osteoarthritis 49 nephrosis 49 developmental disability 49 deafness blindness 49 encephalitis meningitis 49 epigenetic changes 49 Lichen planus 49 Demographers attribute 49 aplastic anemia rare 49 Primary IGFD 49 Preeclampsia 49 Fanconi Anaemia 49 malignant brain 49 Chronic sinusitis 49 congenital cataract 49 degenerative neurological diseases 49 hypophosphatasia 49 placenta accreta 49 Spinal Muscular Atrophy SMA 49 Myocarditis 49 Chronic insomnia 49 Newborn screening 49 polymyalgia 49 cyanotic congenital heart 49 infantile autism 49 Fetal distress 49 Coronary heart 49 endocrine tumors 49 Factor XIII 49 hereditary hemochromatosis 49 esthesioneuroblastoma rare form 49 SHANK3 49 untreated hypothyroidism 49 posterior urethral valves 49 Hemochromatosis 49 Bronchopulmonary Dysplasia 49 chromosomal anomalies 49 Farrah Fawcett dies 49 Hypertrophic Cardiomyopathy HCM