Related by context. All words. (Click for frequent words.) 70 DiGeorge syndrome rare 70 chromosomal defect 69 Joubert syndrome 69 chromosome abnormality 69 genetic abnormality 69 CHARGE syndrome 68 Angelman syndrome 68 holoprosencephaly 67 Dravet syndrome 67 chromosomal abnormality 67 DiGeorge Syndrome 67 DiGeorge syndrome 67 chromosomal disorders 67 congenital disorder 67 Angelman Syndrome 66 osteogenesis imperfecta 66 genetic disorder 65 biliary atresia 65 spastic diplegia 65 mitochondrial disease 65 Hurler Syndrome 65 Fragile X Syndrome 65 rare chromosomal disorder 65 neural tube defect 65 neurodevelopment disorder 65 Sanfilippo Syndrome 64 chromosomal anomaly 64 genetic syndromes 64 anencephaly 64 Gestational diabetes 64 achondroplasia 64 Congenital Adrenal Hyperplasia 64 Marfan Syndrome 64 MCADD 64 septo optic dysplasia 64 Apert syndrome 64 Spina bifida 64 Joubert Syndrome 64 Polycystic kidney disease 64 pyloric stenosis 64 Prader Willi syndrome 64 ectodermal dysplasia 64 neurodevelopmental disorder 64 bronchopulmonary dysplasia 64 Rubinstein Taybi syndrome 64 trisomy 63 hydrops 63 degenerative disorder 63 congenital adrenal hyperplasia 63 retinal dysfunction 63 Hirschsprung disease 63 Trisomy 63 Hypoplastic Left Heart 63 Pre eclampsia 63 Fanconi anemia 63 Spinal muscular atrophy 63 static encephalopathy 63 medium chain acyl 63 Krabbe Disease 63 hypotonia 63 Prader Willi 63 polycystic ovary syndrome 62 Usher Syndrome 62 congenital diaphragmatic hernia 62 Cerebral palsy 62 Chiari Malformation 62 inherited mutations 62 Noonan Syndrome 62 Retinoblastoma 62 hereditary disorder 62 neuropsychiatric disorder 62 congenital adrenal hyperplasia CAH 62 polycystic ovaries 62 Klinefelter syndrome 62 Rett syndrome neurological disorder 62 congenital deafness 62 Anencephaly 62 Hurler syndrome 62 Diamond Blackfan anemia 62 Moebius Syndrome 62 arthrogryposis 62 juvenile myelomonocytic leukemia 62 congenital anomaly 62 metabolic disorder 62 Down syndrome chromosomal disorder 62 Beckwith Wiedemann syndrome 62 VCFS 62 galactosemia 62 brain malformation 62 amniotic fluid embolism 62 Sanfilippo syndrome 62 degenerative neurological disease 61 congenital abnormality 61 TTTS 61 Von Willebrand disease 61 Niemann Pick disease 61 Rett syndrome 61 Down syndrome 61 skeletal dysplasia 61 clotting disorder 61 diaphragmatic hernia 61 neonatal encephalopathy 61 neuro degenerative disorder 61 Diamond Blackfan Anemia 61 CdLS 61 prenatally diagnosed 61 Treacher Collins syndrome 61 chromosomal defects 61 WAGR syndrome 61 epidermolysis bullosa EB 61 neurobiological disorder 61 Krabbe Leukodystrophy 61 developmental abnormalities 61 hyperemesis 61 persistent pulmonary hypertension 61 MCAD deficiency 61 autism neurological disorder 60 developmental delays 60 Lafora disease 60 truncus arteriosus 60 Tay Sachs disease 60 Pervasive Developmental Disorder 60 enzyme deficiency 60 autistic traits 60 spastic cerebral palsy 60 polycystic ovarian syndrome PCOS 60 Hyperthyroidism 60 neurodegenerative disorder 60 craniosynostosis 60 Goldenhar syndrome 60 NF2 60 polydactylism 60 Hirschsprung Disease 60 polycystic ovarian syndrome 60 Polycystic ovary syndrome PCOS 60 Osteogenesis Imperfecta 60 Krabbe disease 60 Hutchinson Gilford Progeria 60 #q#.# deletion syndrome 60 Aicardi Syndrome 60 chiari malformation 60 aneuploidies 60 Brugada Syndrome 60 placental abruption 60 hypertrophic cardiomyopathy HCM 60 ambiguous genitalia 60 profound deafness 60 AAT deficiency 60 Morquio syndrome 60 Progeria 60 Holoprosencephaly 60 myotonic dystrophy 60 blastoma 60 polycystic ovary syndrome PCOS 60 spinocerebellar ataxia 60 congenital disorders 60 myelomeningocele 60 inherited neurological disorder 60 dyskeratosis congenita 60 Li Fraumeni syndrome 60 Perthes disease 60 placenta praevia 60 degenerative neurological disorder 60 Chiari malformation 59 hemophagocytic lymphohistiocytosis 59 pulmonary atresia 59 recessive genetic 59 verbal apraxia 59 Dwarfism 59 dominantly inherited 59 Crouzon Syndrome 59 cerebellar hypoplasia 59 lymphangioleiomyomatosis LAM 59 Alport Syndrome 59 genetic defect 59 Medulloblastoma 59 endocrine disorder 59 Marfan 59 hyperemesis gravidarum 59 Rh incompatibility 59 biliary atresia rare 59 Polycystic Ovary Syndrome 59 congenital anomalies 59 Aicardi syndrome 59 malformation 59 chromosomal abnormalities 59 Hypothyroidism 59 familial adenomatous polyposis 59 hydrocephaly 59 optic nerve hypoplasia 59 HELLP 59 enterocolitis 59 neurofibromatosis 59 de novo mutations 59 Pompe Disease 59 autoimmune thyroiditis 59 Apert Syndrome 59 ADPKD 59 dysmorphic features 59 Muscular dystrophy 59 Severe Combined Immunodeficiency 59 leukodystrophy 59 Hutchinson Gilford Progeria Syndrome 59 Aplastic anemia 59 atresia 59 autistic tendencies 58 blood clotting disorder 58 polyhydramnios 58 congenital muscular dystrophy 58 Polycystic Ovarian Syndrome PCOS 58 Severe Primary IGFD 58 bladder exstrophy 58 Hashimoto thyroiditis 58 Preeclampsia 58 Wilms tumor 58 ARVD 58 uterus didelphys 58 Apert 58 congenital abnormalities 58 autosomal recessive 58 Beckwith Wiedemann Syndrome 58 Hip dysplasia 58 mitochondrial myopathy 58 bicuspid valve 58 dysautonomia 58 Vitamin B# deficiency 58 Angelman 58 fibrodysplasia ossificans progressiva FOP 58 neurodevelopmental disorders 58 hemolytic disease 58 Crouzon syndrome 58 Myocarditis 58 hormonal disorder 58 quadriplegic cerebral palsy 58 Hutchinson Gilford progeria 58 transfusion syndrome 58 fatal neuromuscular disorder 58 Treacher Collins 58 NF1 58 Cardiomyopathy 58 muscle degeneration 58 torticollis 58 recessive inheritance 58 congenital malformations 58 unprovoked seizures 58 neuro developmental disorder 58 molar pregnancy 58 fibrous dysplasia 58 autosomal recessive disease 58 autosomal recessive genetic 58 Arnold Chiari Malformation 58 childhood disintegrative disorder 58 Prader Willi Syndrome 58 pseudotumor cerebri 58 spinal muscular atrophy 58 Cockayne syndrome 58 psychosocial dwarfism 58 peripartum cardiomyopathy 58 apraxia 58 incurable neurological disorder 58 extreme prematurity 58 hereditary deafness 58 genetically inherited 58 Essential tremor 58 Postpartum depression 58 lissencephaly 58 Moebius syndrome 58 Treacher Collins Syndrome 58 diabetes insipidus 58 Obsessive compulsive disorder 57 dyscalculia 57 Proteus syndrome 57 Endometrial cancer 57 cerebal palsy 57 dilated cardiomyopathy 57 Eloysa Vasquez 57 Long QT syndrome 57 Reactive Attachment Disorder 57 medulloblastoma tumors 57 precocious puberty 57 Hoarseness 57 recessive trait 57 Osteosarcoma 57 congenital hydrocephalus 57 abnormalities 57 sirenomelia 57 cystic fibrosis hereditary 57 congenital hypothyroidism 57 deafness neurological 57 vasa previa 57 MECP2 gene 57 polycystic kidneys 57 incurable neurodegenerative disease 57 IgA deficiency 57 Dravet Syndrome 57 toxoplasmosis 57 cryptorchidism 57 chromosome deletion 57 CHDs 57 neurological disorder affecting 57 Beta thalassemia 57 IUGR 57 severe aplastic anemia 57 Klinefelter Syndrome 57 mental retardation epilepsy 57 autosomal dominant disorder 57 syndrome FAS 57 genetic abnormalities 57 HGPS 57 Becker muscular dystrophy 57 tricuspid atresia 57 CHD7 57 mitochondrial disorder 57 spinal bifida 57 Iron deficiency anemia 57 spastic paraplegia 57 toxemia 57 fronto temporal dementia 57 gestational diabetes mellitus 57 Oppositional Defiant Disorder 57 Asperger Disorder 57 prematurity ROP 57 Morquio Syndrome 57 Premature birth 57 Marfan syndrome 57 Bacterial vaginosis 57 choriocarcinoma 57 ataxia telangiectasia 57 Proteus Syndrome 57 nonalcoholic cirrhosis 57 polymorphic ventricular tachycardia 57 Von Hippel Lindau 57 hereditary hemorrhagic telangiectasia 57 thyroid hormone deficiency 57 developmental disorder 57 Alopecia Areata 57 neurodevelopmental 57 lactase deficiency 57 progeria rare 57 Primary IGFD 57 Arthrogryposis 57 beta thalassemia 57 mitochondrial diseases 57 preeclampsia 57 intraventricular hemorrhage 57 Anorexia nervosa 57 Mitochondrial Disease 57 thyroid dysfunction 57 chromosome abnormalities 57 complex neurobiological disorder 57 Dysplasia 57 recurrent miscarriages 57 cardiac channelopathies 57 progressive neurodegenerative disorder 57 Male pattern baldness 57 Cystic fibrosis CF 57 Hyperactivity 57 neuro developmental 57 Biliary Atresia 57 mental retardation blindness 57 ketoacidosis 57 HELLP Syndrome 57 Hemochromatosis 57 Tuberous Sclerosis 57 embryonal rhabdomyosarcoma 57 mitochondrial dysfunction 57 myelogenous leukemia 57 chronic autoimmune disorder 56 arthrogryposis multiplex congenita 56 neuroblastoma 56 Fanconi Anemia 56 Kawasaki Disease 56 Childhood Disorder 56 Kufs disease 56 Goldenhar Syndrome 56 G#S mutation 56 esophageal atresia 56 Erb palsy 56 Postnatal depression 56 autosomal dominant 56 congenital birth defects 56 Diffuse Intrinsic Pontine Glioma 56 disorder thalassemia 56 von Willebrand disease 56 G6PD deficiency 56 autism spectrum disorder 56 DIPG 56 hypothalamic hamartoma 56 Major depressive disorder 56 Wilm tumor 56 Leber Congenital Amaurosis LCA 56 Hypertrophic cardiomyopathy 56 Alagille syndrome 56 Mental retardation 56 thyroiditis 56 achromatopsia 56 antenatal depression 56 mosaicism 56 thrombophilia 56 degenerative neuromuscular disease 56 Downs Syndrome 56 Long QT Syndrome 56 Retinopathy 56 spina bifida 56 PANDAS 56 chronic granulomatous disease 56 Fanconi Anaemia 56 hypoxic ischemic encephalopathy 56 defective gene 56 epididymitis 56 Tetralogy 56 Hydrocephalus 56 Sturge Weber syndrome 56 ependymoma 56 Ehlers Danlos syndrome 56 Wolf Hirschhorn 56 chorioamnionitis 56 multisystem disease 56 FMR1 gene 56 untreated celiac disease 56 Obstructive sleep apnea 56 ASDs 56 progressive neurological disorder 56 recurrent miscarriage 56 LQTS 56 Canavan Disease 56 dwarfism 56 Polycystic Kidney Disease 56 Aspergers Syndrome 56 Wilm Tumor 56 subclinical hypothyroidism 56 Postpartum psychosis 56 systemic scleroderma 56 McCune Albright 56 cerebral palsy 56 Henoch purpura 56 congenital scoliosis 56 cardiomyopathy 56 Folic acid deficiency 56 Krabbe leukodystrophy 56 orchitis 56 Rett Syndrome 56 Autoimmune disorders 56 Pulmonary hypertension 56 Aortic stenosis 56 immunodeficiency disorder 56 Tuberous Sclerosis Complex 56 AAT Deficiency 56 Lesch Nyhan syndrome 56 Fragile X 56 neurological disorder 56 Battens Disease 56 congenital glaucoma 56 Myopathy 56 spinal muscular atrophy SMA 56 congenital CMV 56 renovascular hypertension 56 abnormality 56 syringomyelia 56 Aortic dissection 56 Polycystic ovary syndrome 56 fetal malformations 56 Gastroparesis 56 birth defect 56 Maternal obesity 56 Spinal Muscular Atrophy SMA 56 manic depressive disorder 56 chromosomal anomalies 56 pulmonary hypoplasia 56 cerebral palsy epilepsy 56 hepatoblastoma 56 Coeliac disease 56 hormone imbalances 55 osteopetrosis 55 defects mental retardation 55 Dyspraxia 55 leukoencephalopathy 55 nonsense mutation 55 spastic quadriplegic cerebral palsy 55 brachial plexus palsy 55 Twin Transfusion Syndrome 55 Cushing syndrome 55 Mitochondrial diseases 55 Pompe disease rare 55 HELLP syndrome 55 tuberous sclerosis complex 55 congential 55 Ectodermal Dysplasia 55 recessive gene 55 incurable genetic 55 behavioral disinhibition 55 congenital cataracts 55 SIDS Sudden Infant Death 55 limb deformities 55 Autism Spectrum Disorder 55 Brugada syndrome 55 severe congenital neutropenia 55 pre eclampsia 55 adrenal function 55 HLHS 55 osteosarcoma bone 55 myositis 55 Leber congenital amaurosis 55 Phenylketonuria PKU 55 Parkinson degenerative 55 neurodevelopmental disability 55 infertility miscarriage 55 otosclerosis 55 Heavy menstrual bleeding 55 growth restriction IUGR 55 mitochondrial disorders 55 Combined Immune Deficiency 55 Attention Deficit Hyperactive Disorder 55 Fanconi anemia rare 55 subdural bleeding 55 hypopituitarism 55 primary ciliary dyskinesia 55 Apraxia 55 idiopathic 55 primary ovarian insufficiency 55 juvenile myoclonic epilepsy 55 recurrent abdominal pain 55 Cystic fibrosis 55 cri du chat 55 autism spectrum disorders ASDs 55 primitive neuroectodermal tumors 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 Myotonic dystrophy 55 diagnosed prenatally 55 testicular tumors 55 neuro muscular disorder 55 spinal muscle atrophy 55 SHANK3 55 gestational diabetes 55 congenital cataract 55 Pelizaeus Merzbacher disease 55 cystic fibrosis muscular dystrophy 55 neuroblastoma tumor 55 skeletal abnormalities 55 untreated gonorrhea 55 monozygotic twins 55 genetic mutation 55 Mitochondrial disease 55 phenylketonuria 55 mutated gene 55 Neurofibromatosis 55 carbohydrate intolerance 55 MYH9 gene 55 cardiac hypertrophy 55 cystic fibrosis sickle cell 55 CDH1 55 Usher syndrome 55 leptin deficiency 55 neurobehavioral disorder 55 Wilms Tumor 55 debilitating neurological disorder 55 immunodeficiencies 55 lymphoblastic lymphoma 55 MeCP2 gene 55 hypothyroidism 55 twin transfusion 55 congenital defects 55 arrhythmogenic right 55 roseola 55 intrauterine infection 55 Sudden infant 55 cerebellar ataxia 55 atopic eczema 55 fatal neurodegenerative disorder 55 alzheimer disease 55 gastrointestinal dysfunction 55 Huntington Chorea 55 craniopagus parasiticus 55 hereditary predisposition 55 pre eclamptic 55 nutritional deficiency 55 incompetent cervix 55 Asberger Syndrome 55 VUR 55 situs inversus 55 dyspraxia 55 neurological abnormalities 55 congenital heart 55 severe dehydrating diarrhea 55 microcephaly 54 FXTAS 54 gastroschisis 54 irregular menstrual cycles 54 petit mal seizures 54 Dilated cardiomyopathy 54 encephalitis meningitis 54 Asperger disorder 54 hereditary disorders 54 underactive thyroid gland 54 Fragile X syndrome 54 aneuploidy 54 Diabetic Ketoacidosis 54 adrenoleukodystrophy ALD 54 osteogenesis imperfecta OI 54 nerve palsy 54 Sudden Unexplained Death 54 undiagnosed celiac disease 54 Chronic fatigue 54 Leber congenital amaurosis LCA 54 CMV infection 54 de ath 54 aortic rupture 54 gene mutation 54 involuntary tics 54 cystic kidney 54 Porphyria 54 immunodeficiency 54 polydactyly 54 dysphasia 54 Lactose intolerance 54 neurofibroma 54 idiopathic epilepsy 54 anovulation 54 alveolar rhabdomyosarcoma 54 Biliary atresia 54 muscular dystrophy cystic fibrosis 54 Von Willebrand 54 epidermolysis bullosa 54 Uterine fibroids 54 Rh positive 54 placenta previa 54 mitochondrial mutations 54 kernicterus 54 JMML 54 SRBD 54 Cholangiocarcinoma 54 von Hippel Lindau 54 histiocytosis 54 Sandhoff disease 54 tic disorder 54 meningitis encephalitis 54 disease NAFLD 54 teratoma 54 ocular albinism 54 discoid lupus 54 Toxoplasmosis 54 malformations 54 habitual snoring 54 paraneoplastic 54 familial hypercholesterolemia 54 autosomal dominant inheritance 54 Leber hereditary optic neuropathy 54 Menkes disease 54 Parkinson disease neurodegenerative disorder 54 autosomal recessive disorder 54 hormonal abnormalities 54 hemochromatosis 54 JAK mutations 54 PPCM 54 autistic regression 54 insulin resistance syndrome 54 craniofacial abnormalities 54 Shy Drager syndrome 54 Aspergers syndrome 54 Eisenmenger syndrome 54 Fatty liver 54 hereditary nonpolyposis colorectal cancer 54 Iron deficiency 54 Post partum depression 54 hyperinsulinism 54 Hypophosphatasia 54 blindness deafness 54 Fetal Alcohol Syndrome 54 Retinitis pigmentosa 54 polymyalgia 54 SADS 54 TACI mutations 54 Acute Myeloid Leukaemia 54 Bedwetting 54 neurological complications 54 proximal femoral focal 54 postpartum hemorrhage 54 spine curvature 54 cerebral palsy neurological disorder 54 microdeletion 54 Wiskott Aldrich Syndrome 54 painful genital sores 54 Adrenoleukodystrophy 54 encephalitis swelling 54 Moyamoya disease 54 cardiomyopathy weakening 54 Spina Bifida 54 leukodystrophies 54 PDD NOS 54 post natally 54 developmental disorders 54 Hemolytic Uremic Syndrome HUS 54 congenital malformation 54 Tay Sachs Disease 54 enterovirus infection 54 postoperative delirium 54 inherited neurodegenerative 54 abruption 54 Langerhans cell histiocytosis 54 perinatal depression 54 HNPCC 54 Dystonia 54 Atopic dermatitis 54 Asberger syndrome 54 metabolic abnormality 54 Ewing sarcoma bone 54 Motor neurone disease 54 imperforate anus 54 placental insufficiency 54 disorders ASD 54 Niemann Pick 54 mental retardation cerebral palsy 54 herpes simplex encephalitis 54 Sporadic CJD 54 folic acid deficiency 54 familial adenomatous polyposis FAP 54 variable immunodeficiency 54 predisposing factor 54 multisystem disorder 54 Reye syndrome rare 54 puerperal psychosis 54 T1DM 54 Sudden Arrhythmia Death 53 Osteogenesis imperfecta 53 sporadic ALS 53 carcinoid tumor 53 cortical dysplasia 53 Kenadie 53 Thrombocytopenia 53 Meckel Gruber 53 fat malabsorption 53 untreated hypothyroidism 53 premature birth 53 Peripheral neuropathy 53 Genital herpes 53 Insulin resistance 53 autism spectrum disorders 53 Pervasive Developmental Disorders 53 RPE# 53 gene MECP2 53 nephritis 53 chromosomal imbalance 53 Autistic Spectrum Disorder 53 congenital cytomegalovirus 53 Intussusception 53 Peutz Jeghers syndrome 53 neuroblastomas 53 cardio myopathy 53 PKU genetic 53 primary pulmonary hypertension 53 neurofibromatosis genetic disorder 53 CNTNAP2 53 Acromegaly 53 perinatal asphyxia 53 biochemical imbalance 53 Genetic predisposition 53 ADA SCID 53 muscle hypertrophy 53 ectopic pregnancies 53 PCOD 53 atrioventricular septal defect 53 autosomal dominant polycystic kidney 53 cause cardiac channelopathies 53 inherited genetic mutation 53 fatal neurodegenerative 53 gestational diabetes mellitus GDM 53 enuresis 53 Hypospadias 53 dysgenesis 53 Chronic constipation 53 CFTR gene 53 progressive degenerative neurological 53 nerve degeneration 53 savant syndrome 53 acute rheumatic fever 53 hippocampal function 53 Irritable bowel syndrome 53 Hyperkalemia 53 Hypoglycemia 53 Langerhans Cell Histiocytosis 53 hypophosphatasia 53 juvenile rheumatoid arthritis 53 long QT syndrome 53 epigenetic changes 53 Foetal Alcohol Spectrum Disorder 53 lymphoblastic leukemia 53 intra uterine 53 velo cardio facial 53 fibromatosis 53 fetal abnormalities 53 Pneumococcal meningitis 53 Attention Deficit Disorder ADD 53 eosinophilic esophagitis 53 necrotizing enterocolitis 53 apolipoprotein E gene 53 Gestational Diabetes 53 Syringomyelia 53 irregular menstrual periods 53 combined immunodeficiency SCID 53 hereditary hemochromatosis 53 dysphonia 53 Fragile X gene 53 Rotavirus infection 53 chronic lymphocytic 53 fatty liver disease 53 Duchene muscular dystrophy 53 neurodevelopmental impairment 53 placental malaria 53 xeroderma pigmentosum 53 Marfan syndrome connective tissue 53 enlarged tonsils 53 Generalized anxiety disorder 53 airway blockage 53 Septicaemia 53 Glioma 53 craniofacial anomalies 53 congenital blindness 53 microchimerism 53 monozygotic twin 53 hypertrophic cardiomyopathy 53 degenerative muscular 53 cholestasis 53 associated tremor ataxia 53 ruptured brain aneurysm 53 Fibrosis 53 Syndrome SADS 53 Cowden syndrome 53 sacral agenesis 53 inherited retinal degeneration 53 persistent genital arousal 53 aetiological 53 unexplained infertility 53 preeclamptic 53 Sensorineural hearing loss 53 singleton pregnancy 53 fetal anomalies 53 underactive thyroid 53 overactive thyroid gland 53 Excessive daytime sleepiness 53 neurological degeneration 53 Smith Magenis syndrome 53 Eclampsia 53 coma convulsions 53 recurrent wheezing 53 Diabetic neuropathy 53 aplastic anemia rare 53 lysosomal storage diseases 53 exotropia 53 recessive dystrophic epidermolysis bullosa 53 eclampsia 53 intersexuality 53 defects CHDs 53 Appendicitis 53 Acid reflux 53 progranulin mutations 53 heterotaxy 53 highly heritable 53 Idiopathic Thrombocytopenic Purpura ITP 53 polycystic disease 53 Korsakoff syndrome 53 pelvic inflammatory disease 53 Hemophilia B 53 epilepsy 53 Perthes Disease 53 subdural haemorrhage 53 Parkinson disease neurological disorder 53 postpartum mood 53 Hemiplegia 53 KIBRA 53 genetic defects 53 optic atrophy 53 fatal myelination disorder 53 heart syndrome HLHS 53 idiopathic scoliosis 53 preterm deliveries 53 Mermaid Syndrome 53 abnormal genital 53 paraganglioma 53 HMGA2 53 Churg Strauss syndrome 53 narcolepsy cataplexy 53 mastocytosis 53 genes predisposing 53 nongenetic 53 ventricular dysplasia 53 genetic neuromuscular disorder 53 Secondhand smoke exposure 53 Polycystic ovarian syndrome 53 Wernicke Korsakoff syndrome 53 Alport syndrome 53 premature ovarian 53 bone deformities 53 spinocerebellar ataxia type 53 lichen planus 53 APOE e4 52 ceroid lipofuscinosis NCL 52 febrile seizure 52 post partum psychosis 52 lethargy irritability 52 skeletal malformations 52 cystic fibrosis Duchenne muscular 52 mental retardation 52 Autistic Disorder 52 haemochromatosis 52 microtia 52 autism cerebral palsy 52 osteogenic sarcoma 52 generalized epilepsy 52 1 Antitrypsin Deficiency 52 retinitis pigmentosa degenerative 52 Genetic variants 52 hypogonadotropic hypogonadism 52 Rh factor 52 Ewings Sarcoma 52 gynecologic malignancy 52 autism 52 proband 52 measles encephalitis 52 subfertility 52 deformed limbs 52 Kleine Levin 52 abnormal vaginal bleeding 52 posterior urethral valves 52 neurofibromatosis type 52 born prematurely 52 epilepsy cerebral palsy 52 Leber Congenital Amaurosis 52 retinal blastoma 52 severe hyperbilirubinemia 52 obesity insulin resistance 52 Shwachman Diamond Syndrome 52 sCJD 52 necrotising enterocolitis 52 cystic fibrosis chronic pancreatitis 52 genetic disorders 52 hypertrichosis 52 alpha thalassemia 52 Tourette Syndrome neurological disorder 52 respiratory insufficiency 52 ovarian cysts 52 Tuberous sclerosis 52 clefting 52 hormonal imbalance 52 Premature Ovarian Failure 52 hypoplasia 52 hormone thyroxine 52 primordial dwarfism 52 neonatal respiratory distress 52 Necrotizing Fasciitis 52 sporadic Creutzfeldt Jakob 52 reactive attachment 52 chromosome #q#.# [001] 52 monoclonal gammopathy 52 hirsutism 52 glucose intolerance 52 Crigler Najjar syndrome 52 Acute Myelogenous Leukemia 52 bicuspid aortic valve 52 undescended testicle 52 deafness blindness 52 severe obstructive pulmonary 52 Morbid obesity 52 Oppositional Defiant Disorder ODD 52 FSGS 52 PGD PGS 52 Preterm babies 52 Patau syndrome 52 Cerebral malaria 52 cerebral palsy autism 52 pre cancerous lesion 52 rhesus 52 aspergers syndrome 52 placental abnormalities 52 oral clefts 52 Spasticity 52 Reye Syndrome 52 ApoE gene 52 plagiocephaly 52 Coeliac Disease 52 Colorectal cancers 52 fetal chromosomal abnormalities 52 Brittle Bone 52 Autism Spectrum Disorder ASD 52 RDEB 52 juvenile dermatomyositis 52 filaggrin 52 infantile hemangiomas 52 hypoplastic left 52 intractable epilepsy 52 Chronic insomnia 52 Polycystic Ovarian Syndrome 52 rhabdomyosarcoma 52 Systemic lupus erythematosus SLE 52 varicella infection 52 Persistent Sexual Arousal 52 hereditary diseases 52 neurologic symptoms 52 BRCA gene mutation 52 Batten Disease