Related by context. All words. (Click for frequent words.) 67 chromosome abnormality 66 ectodermal dysplasia 65 holoprosencephaly 65 congenital diaphragmatic hernia 65 Sanfilippo Syndrome 64 Chiari Malformation 63 Dravet syndrome 63 genetic syndromes 63 Hirschsprung disease 63 VCFS 63 Niemann Pick disease 62 chromosomal disorder 62 Joubert syndrome 62 hemophagocytic lymphohistiocytosis 62 chromosomal anomaly 62 CHARGE syndrome 62 Down syndrome chromosomal disorder 62 Apert syndrome 62 Hurler syndrome 62 Treacher Collins syndrome 62 Canavan Disease 62 chromosomal defect 61 Alport Syndrome 61 polycystic kidneys 61 spastic diplegia 61 Histiocytosis 61 myelomeningocele 61 Niemann Pick 61 Congenital Adrenal Hyperplasia 61 Alagille syndrome 61 brain malformation 61 Fragile X Syndrome 61 hereditary disorder 61 autosomal dominant polycystic kidney 61 Spinal muscular atrophy 61 gene MECP2 61 Wilms Tumor 61 Anencephaly 61 Marfan Syndrome 60 Wilms Tumour 60 Fanconi anemia 60 ARVD 60 hydrops 60 Hypoplastic Left Heart 60 ataxia telangiectasia 60 undiagnosed celiac disease 60 primary ciliary dyskinesia 60 medium chain acyl 60 pulmonary hypoplasia 60 Usher Syndrome 60 Angelman syndrome 60 hypertrophic cardiomyopathy HCM 60 MCAD deficiency 60 Langerhans cell histiocytosis 60 Sanfilippo syndrome 60 Chiari malformation 60 DiGeorge Syndrome 59 Cockayne syndrome 59 immunodeficiency disorder 59 Wilm tumor 59 Brugada Syndrome 59 TTTS 59 neurofibromatosis NF 59 PIDD 59 genetic disorder 59 Retinoblastoma 59 Krabbe Disease 59 DiGeorge syndrome 59 brachial plexus palsy 59 myelogenous leukemia 59 Rubinstein Taybi syndrome 59 rare chromosomal disorder 59 spastic paraplegia 59 Crouzon syndrome 59 Fanconi Anemia 59 Crouzon Syndrome 59 Perthes disease 59 Hurler Syndrome 59 Pelizaeus Merzbacher disease 59 biliary atresia 59 recessively inherited 59 retinitis pigmentosa degenerative 58 neuro degenerative disorder 58 gastrointestinal dysfunction 58 Cardiomyopathy 58 leukodystrophies 58 Arnold Chiari Malformation 58 Hirschsprung Disease 58 Nephrotic Syndrome 58 blastoma 58 biliary atresia rare 58 eosinophilic esophagitis 58 Klinefelter syndrome 58 Spinal Muscular Atrophy SMA 58 Tuberous Sclerosis Complex 58 Henoch purpura 58 MCADD 58 Brugada syndrome 58 genetic abnormality 58 lysosomal storage diseases 58 degenerative disorder 58 chronic autoimmune disorder 58 congenital disorder 58 autosomal recessive genetic 58 auditory neuropathy 58 Proteus syndrome 58 autosomal dominant disorder 58 Diffuse Intrinsic Pontine Glioma 58 clotting disorder 58 skeletal dysplasia 58 metachromatic leukodystrophy 58 Dysplasia 58 juvenile myelomonocytic leukemia 58 Hashimoto thyroiditis 58 DiGeorge syndrome rare 58 Arnold Chiari 58 incurable neurodegenerative disease 58 amniotic fluid embolism 58 de novo mutations 58 molar pregnancy 58 Apert Syndrome 58 cystic kidney 58 spinal bifida 58 hypothalamic hamartoma 58 neural tube defect 58 dominantly inherited 57 multisystem disease 57 Spina bifida 57 Adrenoleukodystrophy 57 Myocarditis 57 Leber Congenital Amaurosis LCA 57 juvenile dermatomyositis 57 Severe Primary IGFD 57 septo optic dysplasia 57 Treacher Collins 57 Morquio syndrome 57 Langerhans Cell Histiocytosis 57 myotonic dystrophy 57 mitochondrial disease 57 Krabbe Leukodystrophy 57 histiocytosis 57 mitochondrial myopathy 57 neurodevelopment disorder 57 neurodevelopmental disorder 57 Joubert Syndrome 57 spastic cerebral palsy 57 Beckwith Wiedemann Syndrome 57 Biliary Atresia 57 Von Willebrand disease 57 Klinefelter Syndrome 57 medulloblastoma tumors 57 Hydrocephalus 57 Goldenhar Syndrome 57 blood clotting disorder 57 congenital deafness 57 dyskeratosis congenita 57 Angelman Syndrome 57 transfusion syndrome 57 epidermolysis bullosa 57 placenta praevia 57 Crigler Najjar syndrome 57 ependymoma 57 neurogenetic 57 Becker muscular dystrophy 57 Diamond Blackfan Anemia 57 Friedrich Ataxia 57 Tuberous Sclerosis 57 aneuploidies 57 adrenoleukodystrophy ALD 57 degenerative neurological disease 57 HELLP syndrome 57 Ehlers Danlos syndrome 57 optic nerve hypoplasia 57 achondroplasia 57 HELLP 57 incurable neurological disorder 57 Krabbe disease 57 metabolic disorder 57 Acute Myelogenous Leukemia 57 thrombophilia 57 chiari malformation 57 Myasthenia gravis 57 leukodystrophy 57 Astrocytoma 57 Apert 57 congenital hyperinsulinism 57 Beckwith Wiedemann syndrome 57 Ewing sarcoma bone 57 Diamond Blackfan anemia 56 polycystic ovary syndrome 56 chronic granulomatous disease 56 PPCM 56 galactosemia 56 disorder thalassemia 56 prenatally diagnosed 56 fronto temporal dementia 56 variable immunodeficiency 56 Hutchinson Gilford Progeria 56 Brzustowicz 56 cerebellar hypoplasia 56 protein misfolding diseases 56 HGPS 56 Ectopia Cordis 56 spinal muscular atrophy SMA 56 hereditary spastic paraplegia 56 myotonic muscular dystrophy 56 otosclerosis 56 Hypertrophic 56 pulmonary atresia 56 Treacher Collins Syndrome 56 Wiskott Aldrich Syndrome 56 peripartum cardiomyopathy 56 mitochondrial dysfunction 56 truncus arteriosus 56 pseudotumor cerebri 56 Rett syndrome 56 bronchopulmonary dysplasia 56 retinal dysfunction 56 Meckel Gruber 56 Tay Sachs Disease 56 AAT deficiency 56 Patau syndrome 56 IgA deficiency 56 osteogenesis imperfecta 56 sacral agenesis 56 ADPKD 56 chromosomal abnormality 56 diaphragmatic hernia 56 neuro developmental 56 Retinopathy 56 autoimmune thyroiditis 56 diffuse intrinsic pontine glioma 56 cerebal palsy 56 mitochondrial diseases 56 Pre eclampsia 56 neurofibromatosis 56 Reactive Attachment Disorder 56 Li Fraumeni syndrome 56 metabolic abnormality 56 dysautonomia 56 autistic tendencies 56 genetic defect 56 Parkinsons Disease 56 DIPG 56 Myopathy 56 polycystic ovary syndrome PCOS 55 idiopathic pulmonary 55 CdLS 55 mitochondrial disorders 55 myasthenia gravis neuromuscular 55 congenital adrenal hyperplasia CAH 55 recessive genetic 55 Genetic predisposition 55 severe aplastic anemia 55 Severe Combined Immunodeficiency 55 Aicardi syndrome 55 Tuberous sclerosis 55 discoid lupus 55 Hypophosphatasia 55 choriocarcinoma 55 bladder exstrophy 55 FSGS 55 CHDs 55 Polycystic Kidney Disease 55 lymphoblastic lymphoma 55 hypertrophic obstructive cardiomyopathy 55 epidermolysis bullosa EB 55 Ehlers Danlos Syndrome 55 moyamoya 55 Eisenmenger syndrome 55 HHV 6 55 Sjögren syndrome 55 Myelodysplastic syndrome 55 Porphyria 55 hereditary degenerative 55 Shwachman Diamond Syndrome 55 microchimerism 55 ocular albinism 55 untreated celiac disease 55 MELAS 55 Osteogenesis Imperfecta 55 petit mal seizures 55 acute psychosis 55 quadriplegic cerebral palsy 55 Alopecia Areata 55 neuropsychiatric disorder 55 sporadic Creutzfeldt Jakob 55 Acute Leukemia 55 Krabbe leukodystrophy 55 degenerative neurological disorder 55 placental abruption 55 Tourette Syndrome TS 55 immunodeficiencies 55 mosaicism 55 Neurofibromatosis Type 55 Goldenhar syndrome 55 LQTS 55 progressive neurodegenerative disorder 55 developmental abnormalities 55 connective tissue disorder 55 Rh incompatibility 55 twin transfusion 55 Six3 55 profound deafness 55 Arthrogryposis 55 Friedreich 55 cystic fibrosis hereditary 55 systemic mastocytosis 55 Duchene muscular dystrophy 55 Epstein Barr virus EBV 55 Fanconi 55 chorioamnionitis 55 carcinoid cancer 55 tuberous sclerosis complex 55 Wilm Tumor 55 hepatoblastoma 55 CHD7 55 Mitochondrial disease 55 chromosome #q#.# [001] 55 congenital muscular dystrophy 55 Ehlers Danlos 55 Medulloblastoma 55 Pompe Disease 55 inflammatory demyelinating 55 retinitis pigmentosa RP 55 uterine tumors 55 Arteriovenous Malformation 55 Prader Willi syndrome 55 Angelman 55 precocious puberty 55 arthrogryposis 55 Dravet Syndrome 55 Polycystic kidney disease 55 hormonal disorder 54 Lou Gherig disease 54 Sclerosing 54 osteogenic sarcoma 54 myeloid leukemia 54 inherited retinal 54 Leber congenital amaurosis 54 spinocerebellar ataxia 54 hypothalamic pituitary adrenal axis 54 Lafora disease 54 cerebellar ataxia 54 craniofacial abnormalities 54 Aplastic Anemia 54 hyperparathyroidism 54 MYCN amplification 54 autism neurological disorder 54 Guillain Barré Syndrome 54 Klippel Trenaunay Syndrome 54 AAT Deficiency 54 esophageal atresia 54 osteopetrosis 54 clinically heterogeneous 54 Pervasive Developmental Disorder 54 Long QT Syndrome 54 Hemochromatosis 54 pyloric stenosis 54 verbal apraxia 54 acute myocarditis 54 Arthrogryposis Multiplex 54 NF1 54 congenital disorders 54 JMML 54 Burkitt Lymphoma 54 autosomal recessive disease 54 incurable genetic 54 renovascular hypertension 54 Dwarfism 54 Rett syndrome neurological disorder 54 Lou Gehrigs disease 54 idiopathic dilated cardiomyopathy 54 varicella infection 54 Atresia 54 arthrogryposis multiplex congenita 54 Epstein Barr Virus 54 lymphocytic leukemia 54 nephrosis 54 Fanconi Anaemia 54 toxemia 54 Ataxia Telangiectasia 54 embryonal rhabdomyosarcoma 54 Hemophilia B 54 Tay Sachs disease 54 Pulmonary hypertension 54 myelodysplasia 54 Aicardi Syndrome 54 Usher syndrome 54 immunodeficiency 54 neurodevelopmental disability 54 Retinitis Pigmentosa RP 54 bicuspid valve 54 osteogenesis imperfecta OI 54 haemochromatosis 54 Interstitial cystitis 54 Alport syndrome 54 hereditary hemorrhagic telangiectasia 54 Wegener granulomatosis 54 Autoimmune disorders 54 Acute Myeloid Leukaemia 54 Marfan 54 Dystrophy 54 narcolepsy cataplexy 54 osteosarcoma bone 54 Hutchinson Gilford progeria 54 bicuspid aortic valves 54 lymphoblastic leukemia 54 progressive retinal degenerative 54 adrenal function 54 Long QT syndrome 54 undiagnosed untreated 54 thyroid dysfunction 54 Kawasaki Disease 54 Friedreich ataxia 54 progressive neuromuscular 54 cardiac channelopathies 54 Ventricular Septal Defect 54 ventricular dysplasia 54 Hemolytic Uremic Syndrome 54 Moebius Syndrome 54 Celiac sprue 54 Holoprosencephaly 54 cytomegalovirus infection 54 fungal meningitis 54 Graft Versus Host 54 PPHN 54 Wiskott Aldrich syndrome 54 beta thalassemia 54 aniridia 54 Neurofibromatosis type 54 Neurocognitive 54 Fragile X. 54 vascular birthmarks 53 HNPCC 53 developmental delays 53 Eosinophilic Esophagitis 53 imperfecta 53 optica 53 Sudden Arrhythmia Death 53 fibrous dysplasia 53 Sturge Weber syndrome 53 precancerous cervical 53 SMN protein 53 Preeclampsia 53 Raynaud disease 53 Velculescu 53 velo cardio facial 53 Hypertrophic Cardiomyopathy 53 degenerative muscular 53 herpes encephalitis 53 Fragile X syndrome 53 thoracic aortic disease 53 achromatopsia 53 Endometrial cancer 53 nephrogenic 53 optic atrophy 53 retinal degenerative disease 53 reproductive endocrine 53 nonhereditary 53 dysgenesis 53 Chronic fatigue 53 Maroteaux Lamy syndrome 53 static encephalopathy 53 Leber congenital amaurosis LCA 53 Crohns Disease 53 neurodevelopmental 53 alpha1 antitrypsin deficiency 53 Osteogenesis imperfecta 53 Wilms tumors 53 congenital birth defects 53 congenital abnormality 53 inherited mutations 53 pulmonary hypertension PH 53 hyperemesis 53 neonatal encephalopathy 53 lymphangioleiomyomatosis LAM 53 neurofibromatosis type 53 muscular dystrophy cystic fibrosis 53 Pervasive Developmental Disorders 53 Fragile X 53 mental retardation blindness 53 haemolytic uraemic syndrome 53 Morquio 53 familial ALS 53 congenita 53 neuro developmental disorder 53 multiforme 53 neuro degenerative 53 spinal muscle atrophy 53 alveolar rhabdomyosarcoma 53 xeroderma pigmentosum 53 leukoencephalopathy 53 disorders FASD 53 tricuspid atresia 53 systemic scleroderma 53 malformation 53 LRRK2 mutations 53 neurological sequelae 53 Parkinson degenerative 53 chromosomal disorders 53 renal scarring 53 1 Antitrypsin Deficiency 53 JAK2 mutation 53 inherited neurological disorder 53 Irlen Syndrome 53 borderline mental retardation 53 dilated cardiomyopathy 53 polycystic ovarian syndrome PCOS 53 post transplant lymphoproliferative 53 herpesviruses 53 HIBM 53 Acute Myeloid Leukaemia AML 53 rheumatic disease 53 multisystem disorder 53 genetic neuromuscular disorder 53 immuno deficiency 53 uterus didelphys 53 Glioma 53 SADS 53 parathyroid carcinoma 53 cortical dysplasia 53 Niemann Pick Disease 53 Hutchinson Gilford Progeria Syndrome 53 Cystic Fibrosis CF 53 idiopathic cardiomyopathy 53 lichen planus 53 GPC5 53 Ichthyosis 53 Polycystic ovary syndrome PCOS 53 Polymorphic Ventricular Tachycardia CPVT 53 persistent pulmonary hypertension 53 debilitating neurological disease 53 chronic renal disease 53 polycystic ovarian syndrome 53 behavioral disinhibition 53 cryptococcal meningitis 53 Pompe disease rare 53 intractable epilepsy 53 late onset Pompe 53 Kleine Levin 53 Aplastic anemia 53 postpartum hemorrhage 53 Cowden syndrome 53 mGluR5 antagonist 53 Myositis 53 polymyalgia rheumatica 53 congenital glaucoma 53 cystic fibrosis 53 Tourette syndrome neurological disorder 53 lissencephaly 53 Myalgic Encephalomyelitis 53 G6PD deficiency 53 MECP2 gene 53 familial dysautonomia 53 medulloblastomas 53 fatal neuromuscular disorder 53 Major depressive disorder 53 Idiopathic Thrombocytopenic Purpura ITP 53 Hereditary angioedema 53 cystic fibrosis muscular dystrophy 53 Osteosarcoma 53 recurrent miscarriage 53 Cryptococcus neoformans 53 Mucopolysaccharidosis 53 Dystonia 53 Transverse Myelitis 53 Autistic Spectrum Disorder 53 Juvenile Rheumatoid Arthritis 53 aplastic anemia 52 multisystemic 52 Moyamoya 52 Aspergers Syndrome 52 Leber hereditary optic neuropathy 52 Arrhythmogenic Right Ventricular Cardiomyopathy 52 Neurofibromatosis 52 Premature Ovarian Failure 52 WDR# 52 Meniere Disease 52 Ebstein anomaly 52 arrhythmogenic right 52 Cerebral palsy 52 autoimmune hemolytic anemia 52 spinal muscular atrophy 52 Acute Lymphoblastic Leukaemia 52 progressive neurodegenerative 52 ruptured brain aneurysm 52 Familial hypercholesterolemia 52 neurocognitive deficits 52 JAK mutations 52 neuro degenerative disease 52 Familial Dysautonomia 52 Relling 52 degenerative neurological condition 52 Ectodermal Dysplasia 52 neurodevelopmental outcomes 52 Bardet Biedl syndrome 52 neurologic deficits 52 Ataxia 52 Hypertrophic cardiomyopathy 52 PTLD 52 Wilms tumor 52 Reflex Sympathetic Dystrophy RSD 52 Leukodystrophy 52 Newborn screening 52 myalgic encephalomyelitis ME 52 Alzheimers disease 52 Inflammatory bowel diseases 52 systemic amyloidosis 52 hydrocephaly 52 neurological complications 52 Alzhiemer 52 spontaneous mutation 52 congential 52 del 5q 52 diffuse pontine glioma 52 cardio myopathy 52 cerebral palsey 52 Polycystic Ovary Syndrome 52 sporadic ALS 52 Acute Lymphocytic Leukemia 52 necrotizing enterocolitis 52 interstitial pulmonary fibrosis 52 idiopathic scoliosis 52 multiple sclerosis lupus 52 FMR1 gene 52 Prader Willi 52 cystic fibrosis Duchenne muscular 52 recurrent miscarriages 52 Korsakoff syndrome 52 spastic diplegia cerebral palsy 52 Obstructive Sleep Apnoea 52 vasa previa 52 hereditary nonpolyposis colorectal cancer 52 Persistent Pulmonary Hypertension 52 epilepsy cerebral palsy 52 postoperative delirium 52 autoimmune encephalitis 52 heterotaxy 52 Progeria 52 synovial sarcoma 52 kernicterus 52 neurodevelopmental disorders 52 Fatty liver 52 gastric carcinoma 52 idiopathic epilepsy 52 thiopurine 52 Oesophageal 52 dystrophy 52 enzyme deficiency 52 Mitochondrial diseases 52 inherited metabolic disorders 52 Thrombocytopenia 52 Barth Syndrome 52 Morquio Syndrome 52 craniosynostosis 52 Sjogren Syndrome 52 Hyperkalemia 52 autosomal dominant 52 aplastic anemia rare 52 lysosomal storage disease 52 Ewings Sarcoma 52 FXTAS 52 hereditary disorders 52 cardiomyopathy weakening 52 paraneoplastic 52 neurodegenerative disorder 52 Leber Hereditary Optic Neuropathy 52 #q#.# deletion syndrome 52 Congenital Muscular Dystrophy 52 puerperal psychosis 52 hemolytic anemia 52 POAG 52 polyhydramnios 52 spontaneous remission 52 Duchene Muscular Dystrophy 52 torticollis 52 Hypothyroidism 52 Duchenne Muscular Dystrophy DMD 52 neurofibromatosis genetic disorder 52 Cushing syndrome 52 causative gene 52 enterocolitis 52 nodular melanoma 52 acidemia 52 Nephrogenic Systemic Fibrosis NSF 52 Cockayne Syndrome 52 monoclonal gammopathy 52 Aortic dissection 52 Pseudomonas aeruginosa infections 52 Folic acid deficiency 52 idiopathic thrombocytopenic purpura 52 blood clotting disorders 52 neurocardiogenic syncope 52 agenesis 52 hereditary predisposition 52 mental retardation epilepsy 52 combined immunodeficiency SCID 52 viral myocarditis 52 celebral palsy 52 Acute myeloid leukemia 52 Acidosis 52 Von Willebrand 52 primary ovarian insufficiency 52 Erb palsy 52 placental malaria 52 familial adenomatous polyposis FAP 52 polycystic kidney disease 52 hereditary deafness 52 spastic quadriplegic cerebral palsy 52 NPHP 52 Phenylketonuria PKU 52 Combined Immune Deficiency 52 Postnatal Depression 52 infantile hemangioma 52 G#S mutation 52 Fanconi anemia rare 52 Necrotizing fasciitis 52 EBV infection 52 Glioblastoma Multiforme 52 dissecans 52 Acute Promyelocytic Leukemia 52 IPAH 52 pilocytic astrocytomas 52 necrotizing enterocolitis NEC 52 type 1diabetes 52 intraventricular hemorrhage 52 Vingan 52 Polycystic Ovarian Syndrome PCOS 52 interstitial nephritis 52 progressive neurodegenerative disease 52 congenital anomaly 52 recurrent abdominal pain 52 Muscular dystrophy 52 demyelinating 52 Aortic stenosis 52 Twin Transfusion Syndrome 52 smoldering myeloma 52 NOMID 52 Leukemias 52 pulmonary haemorrhage 52 spina bifida 52 pituitary adenoma 52 epigenetic changes 52 Moyamoya disease 52 mastocytosis 52 chromosome abnormalities 52 thyroid hormone deficiency 52 PGD PGS 52 cerebral palsy neurological disorder 52 prematurity ROP 52 endocrine tumors 52 degenerative neuromuscular disease 52 cortical blindness 52 Trisomy 52 polycystic ovaries 52 post natally 52 incurable degenerative 51 Idiopathic Thrombocytopenic Purpura 51 muscular atrophy 51 Gastroparesis 51 thrombotic thrombocytopenic purpura 51 neurological impairments 51 gene mutation 51 progranulin mutations 51 bicuspid aortic valve 51 Cholangiocarcinoma 51 neuromotor 51 Peutz Jeghers syndrome 51 spastic quadriplegia 51 congenital heart 51 Asperger Disorder 51 Bronchiolitis 51 undescended testes 51 dermatomyositis 51 toxoplasmosis 51 deafness neurological 51 Proteus Syndrome 51 neonatal respiratory distress 51 psychosocial dwarfism 51 Von Hippel Lindau 51 congenital abnormalities 51 retinal degeneration 51 chromosomal anomalies 51 apraxia 51 autoimmune thyroid 51 neuro developmental disorders 51 Diabetic neuropathy 51 Moebius syndrome 51 hypopituitarism 51 NOTCH1 51 B Cell Lymphoma 51 neuroblastoma tumor 51 von Willebrand 51 chromosomal imbalance 51 atypical rhabdoid tumor 51 Cytomegalovirus CMV 51 autosomal recessive 51 hereditary hemochromatosis 51 dyskinetic 51 Kufs disease 51 neurologic disorder 51 Smith Magenis syndrome 51 Idiopathic 51 Pulmonary fibrosis 51 cause cardiac channelopathies 51 recessive trait 51 congenital cataract 51 placenta accreta 51 aspergers syndrome 51 cholestasis 51 debilitating neurological disorder 51 epididymitis 51 cardiac insufficiency 51 CDH1 51 von Hippel Lindau 51 anencephaly 51 motor neurone 51 ovarian malignancy 51 degenerative neurological diseases 51 atresia 51 Hip dysplasia 51 Syringomyelia 51 pigmentosa 51 neuropsychiatric disorders 51 inherited neurodegenerative disorder 51 Brittle Bone 51 Wegener Granulomatosis 51 febrile seizure 51 hypoxic ischemic encephalopathy 51 enteropathy 51 ANCA associated 51 infection progressive multifocal 51 brainstem glioma 51 Magnesium deficiency 51 Bronchiectasis 51 childhood leukemias 51 familial adenomatous polyposis 51 PPID 51 abnormal genital 51 cytogenetic abnormalities 51 roseola 51 GBA mutations 51 papillary carcinoma 51 Cystic fibrosis CF 51 Eosinophilic 51 degenerative neurological 51 obliterative bronchiolitis 51 inherited neurodegenerative 51 Chronic lymphocytic leukemia 51 atrioventricular septal defect 51 myeloproliferative disorder 51 mild mental retardation 51 Foetal 51 IUGR 51 NAGS deficiency 51 hypogonadotropic hypogonadism 51 fetal malformations 51 hypophosphatasia 51 neurological abnormalities 51 recessive dystrophic epidermolysis bullosa 51 severe malignant osteopetrosis 51 CMV infections 51 Retinitis pigmentosa 51 hyperprolactinemia 51 Iron deficiency anemia 51 epilepsy 51 genetic lysosomal storage 51 retinal blastoma 51 deletion 5q 51 hormone imbalances 51 primary IGFD 51 Mitochondrial 51 chiari 51 ectopia cordis 51 Auditory Processing Disorder 51 FMRP protein 51 congenital anomalies 51 sickle cell disease 51 spinocerebellar ataxia type 51 diabetes mellitus DM 51 CFS ME 51 adrenal hormones 51 torn flexor muscle 51 choroidal melanoma 51 testicular germ cell 51 heart syndrome HLHS 51 fibromatosis 51 myeloproliferative neoplasms 51 PNET 51 Parkinsons disease 51 non polyposis colorectal 51 common disabling neurological 51 premature ovarian 51 congenital scoliosis 51 Wolf Hirschhorn 51 carcinoid tumor 51 arterial calcification 51 Hyperplasia 51 Rhabdomyosarcoma 51 Coeliac disease 51 primary sclerosing cholangitis 51 neurobehavioral disorder 51 hemolytic disease 51 defective gene 51 GISTs 51 intracranial haemorrhage 51 Pneumocystis carinii pneumonia 51 cytomegalovirus CMV 51 sCJD 51 ductal adenocarcinoma 51 McCune Albright 51 Congenital Heart Disease 51 neurodevelopmental impairment 51 thyroid deficiency 51 Candidiasis 51 Inflammatory Breast Cancer 51 spine curvature 51 Alzeimer 51 Antiphospholipid Syndrome 51 physiological abnormalities 51 Gender Identity Disorder GID 51 Leber Congenital Amaurosis 51 stem glioma 51 Vitamin D insufficiency 51 Sudden Arrhythmic Death 51 C. trachomatis 51 Cytomegalovirus 51 LVNC 51 preterm deliveries 51 acute lymphoblastic 51 fetal microchimerism 51 Hydrocephalus Foundation 51 Attention Deficit Hyperactive Disorder 51 thrombocytosis 51 Primary Immune Deficiency 51 GH deficiency 51 fetal chromosomal 51 Epidermolysis bullosa 51 hypothalamic amenorrhea 51 Spinal Muscular Atrophy 51 muscle hypertrophy 51 Factor XIII 51 parainfluenza virus 51 diagnosed prenatally 51 Burkitt lymphoma 51 fetal echocardiogram 51 Oppositional Defiant Disorder 51 neurobiological disorders 51 Barrett esophagus precancerous 51 post thrombotic syndrome 51 Beta thalassemia 51 Hereditary angioedema HAE 51 juvenile idiopathic arthritis 51 Hypospadias 51 Parkinson disease neurodegenerative disorder 51 Sandhoff disease 51 IGFD 51 BMPR2 51 degenerative nerve disorder 51 alzheimer disease 51 AUDs 51 blocked fallopian tubes 51 SUDEP 51 trisomy 51 mtDNA mutations 51 precancerous condition 51 alpha thalassemia 51 subaortic stenosis 51 hypotonia 51 congenital hypothyroidism 51 pleural mesothelioma 51 hemochromatosis 51 idiopathic pulmonary arterial hypertension 51 recessive inheritance 51 urinary blockage 51 Budd Chiari syndrome 51 Malformation 51 meningeal 51 herpes infection 50 gastrointestinal stromal tumor 50 brain lesions 50 respiratory gastrointestinal 50 Urticaria 50 Duchenne muscular dystrophy DMD 50 Fibromyalgia syndrome 50 genetic disorders 50 interrupted aortic arch 50 MECP2 50 lactase deficiency 50 Biliary atresia 50 Myelodysplastic Syndrome 50 Fabry Disease 50 hemorrhagic pancreatitis 50 infertility miscarriage 50 PTEN mutations 50 PKU genetic 50 ataxias 50 Churg Strauss syndrome