Related by context. All words. (Click for frequent words.) 68 neurological disorder affecting 68 ectodermal dysplasia 66 CdLS 65 genetic syndromes 65 myelomeningocele 65 Langerhans cell histiocytosis 65 CHDs 65 holoprosencephaly 65 mitochondrial disorders 65 Henoch purpura 64 Alport Syndrome 64 Autism Spectrum Disorders ASD 64 neurogenetic 64 T1DM 64 chromosome abnormality 64 HNPCC 64 CFS ME 64 ependymoma 64 Severe Primary IGFD 63 Autistic Spectrum Disorder 63 prenatally diagnosed 63 Autism Spectrum Disorder 63 Eisenmenger syndrome 63 SIDS Sudden Infant Death 63 Autistic Spectrum Disorders 63 idiopathic pulmonary 63 Sudden Arrhythmia Death 63 congential 63 embryonal rhabdomyosarcoma 63 Rubinstein Taybi syndrome 63 Noonan Syndrome 63 untreated celiac disease 63 autism spectrum disorders ASDs 63 Hutchinson Gilford progeria 63 autosomal dominant polycystic kidney 63 Chiari malformation 63 hereditary predisposition 63 Leber congenital amaurosis LCA 63 Dravet syndrome 62 somatization disorder 62 HELLP 62 Celiac sprue 62 PIDD 62 undiagnosed celiac disease 62 neuro developmental disorder 62 immunodeficiencies 62 Wernicke Korsakoff syndrome 62 tic disorders 62 bicuspid aortic valves 62 Myotonic dystrophy 62 Hurler syndrome 62 Medulloblastoma 62 Von Willebrand disease 62 Pervasive Developmental Disorder 62 Takotsubo cardiomyopathy 62 #q#.# deletion syndrome 62 Sjögren syndrome 62 Phenylketonuria PKU 62 narcolepsy cataplexy 62 paraneoplastic 62 haemochromatosis 62 comorbid anxiety 62 Hemochromatosis 62 smoldering myeloma 62 myalgic encephalomyelitis ME 62 de novo mutations 62 euthymic patients 62 Brugada Syndrome 62 velo cardio facial 62 chronic autoimmune disorder 62 DIPG 62 Autistic Disorder 62 Wiskott Aldrich Syndrome 62 Hirschsprung disease 62 Apert syndrome 62 incurable neurodegenerative disease 62 Tourette Syndrome TS 62 neuro developmental 62 chromosomal disorder 62 aneuploidies 62 Myelodysplastic syndrome 62 fronto temporal dementia 62 neurodevelopmental disorder 61 cleft lip cleft palate 61 underlying pathophysiology 61 Tuberous Sclerosis 61 EoE 61 Parkinsons Disease 61 neuropsychiatric disorder 61 CDH1 61 Dwarfism 61 Angelman syndrome 61 Genetic predisposition 61 ARVD 61 CHARGE syndrome 61 neurological impairments 61 muscular dystrophy cystic fibrosis 61 familial clustering 61 atherothrombosis 61 astrocytomas 61 Retinoblastoma 61 retinal dysfunction 61 Acute Myeloid Leukaemia AML 61 congenital toxoplasmosis 61 Muscular dystrophy 61 Arnold Chiari Malformation 61 primary ciliary dyskinesia 61 Fetal alcohol 61 clinically heterogeneous 61 neuropsychological impairments 61 diabetes mellitus DM 61 myeloproliferative 61 Krabbe Disease 61 affective psychoses 61 Autism Spectrum Disorder ASD 61 thoracic aortic disease 61 autism spectrum disorders 61 Alzheimers Disease 61 Chronic lymphocytic leukemia 61 psychiatric comorbidities 61 Becker muscular dystrophy 61 immunocompetent 61 neurodevelopmental disability 61 dyslexia dyspraxia 61 thrombophilia 61 Polycystic Ovarian Syndrome PCOS 61 diffuse gastric 61 leptin deficiency 61 Wolf Hirschhorn 61 Pervasive Developmental Disorders 61 hemophagocytic lymphohistiocytosis 61 Osteogenesis imperfecta 61 Joubert syndrome 61 autism Asperger 61 Polycystic ovary syndrome PCOS 60 multisystem disease 60 Clinical Trials Consortium 60 DiGeorge Syndrome 60 autism spectrum disorders ASD 60 leukemia lymphomas 60 neurobehavioral disorders 60 Hutchinson Gilford Progeria 60 SADS 60 generalized epilepsy 60 Kleine Levin 60 spastic diplegia 60 craniofacial abnormalities 60 Chiari Malformation 60 progressive degenerative neurological 60 vascular birthmarks 60 neuro degenerative disorder 60 vascular anomalies 60 Cardiomyopathy 60 NOMID 60 Perthes disease 60 Fanconi Anemia 60 Von Hippel Lindau 60 rheumatologic 60 #q# deletion syndrome 60 Major depressive disorder 60 progranulin mutations 60 Ehlers Danlos 60 hypopituitarism 60 deafblindness 60 idiopathic pulmonary arterial hypertension 60 CP CPPS 60 Leber Congenital Amaurosis LCA 60 Spinal muscular atrophy 60 Sanfilippo Syndrome 60 juvenile myelomonocytic leukemia 60 Ectopia Cordis 60 cortical dysplasia 60 DiGeorge syndrome 60 skeletal dysplasia 60 Vitamin B# deficiency 60 systemic autoimmune 60 Leukemias 60 myalgic encephalomyelitis 60 degenerative neurological diseases 60 Crigler Najjar syndrome 60 Irritable bowel syndrome IBS 60 eosinophilic disorders 60 recessively inherited 60 von Hippel Lindau 60 cystic kidney 60 perinatal depression 60 ANCA associated 60 neurodevelopmental disorders 60 Obsessive compulsive disorder 60 thoracic aortic aneurysm 60 neurobiological disorders 60 familial hypercholesterolaemia FH 60 verbal apraxia 60 Angelman Syndrome 60 neuropathologic 60 neurodevelopment disorder 60 untreated OSA 60 obesity insulin resistance 60 McCune Albright 60 Li Fraumeni syndrome 60 Autistic Spectrum 60 Syringomyelia 60 chromosome deletion 60 hyperinsulinism 60 inherited retinal 60 ADPKD 60 Autism Spectrum Disorders ASDs 60 chronic renal disease 60 clefting 60 GH deficiency 60 vWD 60 DVT PE 60 Eosinophilic 60 Friedrich Ataxia 60 autism Asperger Syndrome 60 Meckel Gruber 60 congenital adrenal hyperplasia CAH 60 bladder exstrophy 60 leukodystrophy 59 Spinal Muscular Atrophy SMA 59 premorbid 59 Rh incompatibility 59 chromosomal anomaly 59 familial pancreatic cancer 59 cerebellar hypoplasia 59 developmental disorders 59 Sturge Weber Syndrome 59 NF1 59 autonomic dysfunction 59 autosomal recessive genetic 59 aetiological 59 dominantly inherited 59 Meniere Disease 59 Reactive Attachment Disorder 59 post thrombotic syndrome 59 Sudden Unexplained Death 59 neuropathies 59 AAT deficiency 59 chronic myeloid 59 etiologic factors 59 atherothrombotic 59 cerebral palsy spina bifida 59 neurobiological disorder 59 Dysplasia 59 urolithiasis 59 neurological abnormalities 59 Vulvodynia 59 molar pregnancy 59 High Functioning Autism 59 medulloblastoma malignant brain tumor 59 motor neurone 59 Dental caries 59 inherited mutations 59 antiphospholipid syndrome 59 atypical parkinsonism 59 Gender Identity Disorder 59 somatoform disorders 59 Heavy menstrual bleeding 59 Autism Asperger Syndrome 59 monogenic 59 GPC5 59 thyroid dysfunction 59 familial adenomatous polyposis FAP 59 Polycystic Ovary Syndrome 59 progressive neurodegenerative disorder 59 congenital hyperinsulinism 59 dissociative disorders 59 congenital diaphragmatic hernia 59 recessive inheritance 59 neuromotor 59 transfusion syndrome 59 nonbacterial prostatitis 59 esophageal reflux 59 Lafora disease 59 oligodendrogliomas 59 Epstein Barr Virus 59 Marfan 59 testicular germ cell 59 Premature Ovarian Failure 59 brain malformation 59 myelogenous leukemia 59 Sjogren Syndrome 59 renovascular hypertension 59 postoperative pulmonary 59 hereditary spastic paraplegia 59 congenital deafness 59 polycystic ovary syndrome PCOS 59 dermatitis herpetiformis 59 pulmonary hypertension PH 59 Barth Syndrome 59 IPAH 59 MELAS 59 Interstitial cystitis 59 LHON 59 Cognitive dysfunction 59 post transplant lymphoproliferative 59 supratentorial 59 prostate carcinogenesis 59 Chronic fatigue 59 atypical hemolytic uremic syndrome 59 thyroid hormone deficiency 59 bronchogenic carcinoma 59 Ebstein anomaly 59 Acute myeloid leukemia 59 acute lymphoid leukemia 59 neuro degenerative 59 Primary Immunodeficiency 59 disorder ASD 59 neuritic 59 syncopal 59 LQTS 59 Aortic stenosis 59 PNET 59 Klinefelter Syndrome 59 discoid lupus 59 Angelman 58 enterocolitis 58 #q# deletion 58 ciliopathies 58 SHANK3 gene 58 MYH9 gene 58 fibromatosis 58 epilepsy 58 cerebral palsy Down syndrome 58 comorbid disorders 58 cystic fibrosis muscular dystrophy 58 de ath 58 hypertrophic cardiomyopathy HCM 58 myositis 58 spastic paraplegia 58 mental retardation epilepsy 58 nondemented 58 kernicterus 58 Oppositional Defiant Disorder 58 CHD7 58 chromosome #q#.# [001] 58 myelodysplasia 58 neuro developmental disorders 58 autism spectrum disorder 58 spina bifida cerebral palsy 58 interstitial nephritis 58 mitochondrial mutations 58 primary hyperparathyroidism 58 Essential Tremor 58 inherited neurological disorder 58 Asperger Disorder 58 polycystic kidneys 58 Mitochondrial Disease 58 Aspergers Syndrome 58 PCNSL 58 neurogenic bladder 58 ASDs 58 autosomal dominant disorder 58 chronicity 58 MCAD deficiency 58 Shy Drager syndrome 58 Pre eclampsia 58 medulloblastoma tumors 58 Severe Combined Immunodeficiency 58 autism dyslexia 58 childhood disintegrative disorder 58 PANDAS 58 developmental dyscalculia 58 nonhereditary 58 MPGN 58 AAT Deficiency 58 Coeliac Disease 58 Marfan Syndrome 58 Morquio 58 Wegener granulomatosis 58 Bronchiolitis 58 Usher Syndrome 58 inflammatory demyelinating 58 Myasthenia gravis 58 bacterial prostatitis 58 Wilms tumors 58 Polycystic Kidney Disease 58 Arrhythmogenic Right Ventricular Cardiomyopathy 58 Nephrogenic Systemic Fibrosis NSF 58 mitochondrial dysfunction 58 immunodeficiency disorder 58 Lewy Body 58 behavioral disturbances 58 mental retardation blindness 58 TMJ disorder 58 urological cancers 58 comorbid depression 58 Childhood Disorder 58 myelomas 58 FSGS 58 neurocognitive deficits 58 cystic fibrosis chronic pancreatitis 58 Neurofibromatosis type 58 acute myeloid 58 choriocarcinoma 58 Parkinson Disease PD 58 Ewing sarcoma bone 58 Hashimoto thyroiditis 58 Leber Hereditary Optic Neuropathy 58 neoplastic 58 mental retardation cerebral palsy 58 neurosensory 58 spinocerebellar ataxia 58 intestinal polyps 58 JAK mutations 58 multiple sclerosis cerebral palsy 58 treating sarcoma testicular 58 impaired cognition 58 spontaneous miscarriages 58 internalizing disorders 58 ataxias 58 Anencephaly 58 HIV lipodystrophy 58 psychosocial functioning 58 inguinal hernias 58 APOE ε4 58 motor neuron degeneration 58 Lateral Sclerosis 58 clinicopathological 58 dysphasia 58 Periodontitis 58 neurological sequelae 58 neuropsychiatric diseases 58 optic atrophy 58 persistent pulmonary hypertension 58 bone marrow mesenchymal stem 58 Myositis 58 gene MECP2 58 achondroplasia 58 medically unexplained 58 Myocarditis 58 neurofibromatosis type 58 osteopetrosis 58 1 diabetes T1D 58 ataxia telangiectasia 58 renal scarring 58 spinal muscular atrophy SMA 58 peripartum cardiomyopathy 58 HGPS 58 dyskeratosis congenita 58 skeletal abnormalities 58 Waldenstrom macroglobulinemia 58 Knee osteoarthritis 58 Alzhiemer 58 hereditary hemorrhagic telangiectasia 58 chromosome #q#.# deletion 58 Attention Deficit Hyperactive Disorder 58 sCJD 58 myeloproliferative neoplasms 58 hypercalciuria 58 Myelodysplastic syndromes MDS 58 Pompe Disease 58 neurocognitive dysfunction 58 Cognitive impairment 58 incurable neurological disorder 58 AA Amyloidosis 58 auditory neuropathy 58 systemic scleroderma 58 Fragile X Syndrome 58 neurocognitive impairment 58 GBA mutations 58 chorioamnionitis 58 Hereditary angioedema HAE 58 bipolar illness 58 polycystic ovary syndrome 58 Genetic variants 58 Sudden Arrhythmic Death 58 pediatric cataract 58 hereditary breast 58 medium chain acyl 58 testicular tumors 58 leukodystrophies 58 primary immunodeficiency 58 motor neuron diseases 58 PPCM 58 microdeletion 58 Endometrial cancer 58 autoinflammatory diseases 58 microchimerism 58 TTTS 58 Ectodermal Dysplasia 58 ADHD ADD 58 Ankylosing spondylitis 58 Fatty Liver Disease 58 Meningiomas 57 autistic tendencies 57 Klinefelter syndrome 57 LVNC 57 swallowing disorders 57 T1D 57 XMRV infection 57 inherited retinal degeneration 57 carcinoid 57 MECP2 gene 57 retinal degenerative disease 57 Morquio syndrome 57 bronchopulmonary dysplasia BPD 57 herpes simplex encephalitis 57 chromosomal disorders 57 Nonalcoholic fatty liver 57 Brugada syndrome 57 neurobehavioral disorder 57 Gastroparesis 57 biopsychosocial 57 hypovitaminosis D 57 unexplained mental retardation 57 intracranial hypertension 57 paraganglioma 57 idiopathic epilepsy 57 Glioblastoma Multiforme GBM 57 orofacial pain 57 abdominal abscesses 57 Hypospadias 57 atherosclerotic cardiovascular 57 Aspergers syndrome 57 GISTs 57 gastrointestinal dysfunction 57 Sudden Unexpected Death 57 Sanfilippo syndrome 57 genetic loci 57 Acute Leukemia 57 rare chromosomal disorder 57 childhood leukemias 57 Tay Sachs Disease 57 autoimmune thyroiditis 57 debilitating neurological disease 57 Transverse myelitis 57 fibrous dysplasia 57 progressive neurodegenerative 57 aetiology 57 pituitary adenoma 57 G6PD deficiency 57 Alagille syndrome 57 Moebius syndrome 57 Hypoplastic Left Heart 57 extramedullary 57 Frontotemporal Dementia 57 galactosemia 57 postpartum mood 57 Juvenile Arthritis 57 Dravet Syndrome 57 alexithymia 57 chromosomal anomalies 57 Hypertrophic cardiomyopathy 57 chronic periodontitis 57 subclinical atherosclerosis 57 lissencephaly 57 psoriasis psoriatic arthritis 57 orchitis 57 prematurity ROP 57 SRBD 57 Dyspraxia 57 Niemann Pick disease 57 neurologic disorder 57 neurobehavioural 57 Alzheimer Dementia 57 recurrent miscarriage 57 congenital anomalies 57 Epstein Barr Virus EBV 57 Neurofibromatosis 57 lichen planus 57 Keratoconus 57 Foetal Alcohol Spectrum Disorder 57 Congenital Adrenal Hyperplasia 57 invasive secretory carcinoma 57 Diabetic neuropathy 57 Iron deficiency anemia 57 Soft tissue sarcomas 57 aniridia 57 HIV HCV coinfected 57 muscular dystrophy cerebral palsy 57 Schizoaffective Disorder 57 cholestasis 57 polycystic ovarian syndrome PCOS 57 juvenile idiopathic arthritis 57 Mitochondrial disease 57 insulin resistance syndrome 57 neurodevelopmental impairment 57 degenerative neurological disorder 57 psychiatric disorders 57 sporadic Creutzfeldt Jakob 57 Adult Respiratory Distress 57 neurodevelopmental disorder characterized 57 epidermolysis bullosa EB 57 Scheuermann kyphosis 57 schizophreniform disorder 57 Hypertrophic 57 lipodystrophy syndrome 57 WAGR syndrome 57 alzheimer disease 57 Marfan syndrome 57 Polycythemia vera 57 cleft lips cleft palates 57 Fetal Alcohol Syndrome 57 leukemia lymphoma myeloma 57 gallstone disease 57 cardiac channelopathies 57 Fanconi anemia 57 Pelizaeus Merzbacher disease 57 hydrocephaly 57 Pneumococcal pneumonia 57 autism 57 Wiskott Aldrich syndrome 57 Foetal alcohol 57 Nonalcoholic Fatty Liver Disease 57 lupus scleroderma 57 MCADD 57 rheumatic disease 57 degenerative disorder 57 Juvenile Idiopathic Arthritis JIA 57 epididymitis 57 congenital abnormalities 57 abnormal genital 57 Joubert Syndrome 57 Raynaud disease 57 MGUS 57 HbF 57 tricuspid atresia 57 congenital birth defects 57 Uncontrolled hypertension 57 deafness blindness 57 Posttraumatic Stress Disorder PTSD 57 hypercoagulability 57 infantile hemangiomas 57 Coeliac disease 57 schizophrenia schizoaffective disorder 57 hereditary nonpolyposis colorectal cancer 57 Hp2 2 57 membranous nephropathy 57 idiopathic scoliosis 57 pathophysiologic 57 hay fever allergic rhinitis 57 Pulmonary fibrosis 57 moyamoya 57 pilocytic astrocytomas 57 apraxia 57 multisystemic 57 Cholangiocarcinoma 57 affective psychosis 57 Histiocytosis 57 myeloproliferative neoplasms MPNs 57 osteosarcomas 57 mito 57 Lymphocytic 57 FXTAS 57 muscular dystrophies 57 malignant brain 57 renal fibrosis 57 Brodmann Area 57 sensorineural hearing loss 57 IKZF1 57 cardioembolic stroke 57 bacteraemia 57 kidney insufficiency 57 HHV 6 57 vascular Ehlers Danlos 57 ductal adenocarcinoma 57 occipital regions 57 Myopathy 57 demyelinating 57 ADHD dyslexia 57 Lou Gehrigs disease 57 fatal neuromuscular disorder 57 Chronic Obstructive Pulmonary 57 hemolytic anemia 57 CA MRSA infections 57 Mental retardation 57 Chronic pancreatitis 57 progressive multifocal PML 57 Legg Calvé Perthes disease 57 hypokalemia hypomagnesemia 57 lactose malabsorption 57 LRRK2 mutations 57 von Willebrand Disease 57 multiorgan 57 dysgraphia 57 autism neurological disorder 57 alveolar rhabdomyosarcoma 57 hepatoblastoma 57 hypereosinophilic syndrome 57 myopathies 57 vasa previa 57 hereditary deafness 57 HER2 overexpression 57 sporadic ALS 57 mild cognitive impairments 57 superior mesenteric artery 57 nonalcoholic steatohepatitis 57 susceptibility loci 57 epilepsies 57 unruptured aneurysm 57 Austism 56 disorders FASD 56 Spasticity 56 microdeletions 56 neurologic deficits 56 pulmonary hypoplasia 56 Pemphigus 56 hereditary hemochromatosis 56 TACI mutations 56 bipolar disorder schizophrenia 56 Asperger Syndrome AS 56 Spina bifida 56 Aicardi syndrome 56 Langerhans Cell Histiocytosis 56 limb deformities 56 recessive genetic 56 commonest cause 56 nonalcoholic steatohepatitis NASH 56 de novo AML 56 #p#.# [001] 56 undiagnosed untreated 56 dysgenesis 56 missense mutations 56 lysosomal storage diseases 56 neurofibromatosis NF 56 Glioma 56 Wilm tumor 56 neurodermatitis 56 degenerative neurological disease 56 hypothalamic pituitary adrenal axis 56 Infantile Spasms 56 diagnosable disorder 56 hematopoietic cancers 56 pyloric stenosis 56 juvenile idiopathic arthritis JIA 56 limb girdle muscular dystrophy 56 NF2 56 microscopic colitis 56 Moebius Syndrome 56 Acute Renal Failure 56 polymorphic ventricular tachycardia 56 Compulsive hoarding 56 Hyperkalemia 56 compulsive hoarding 56 Down syndrome chromosomal disorder 56 degenerative neurological 56 Lennox Gastaut syndrome 56 myeloid leukemia 56 essential thrombocythemia 56 renal allograft 56 epilepsy cerebral palsy 56 Autoimmune disorders 56 pleural mesothelioma 56 Dystonia 56 histiocytosis 56 precancerous tumors 56 varicella infection 56 neonatal encephalopathy 56 proliferative retinopathy 56 Cowden syndrome 56 dysthymic disorder 56 Leber congenital amaurosis 56 portal vein thrombosis 56 Acute Promyelocytic Leukemia 56 Vingan 56 Hip fracture 56 Balamuthia 56 fibroids endometriosis 56 deafness neurological 56 anosognosia 56 KRAS oncogene 56 eosinophilic esophagitis 56 Cystic 56 spongiform encephalopathies 56 muscular skeletal disorders 56 Fragile X. 56 compulsive hoarding syndrome 56 Niemann Pick 56 TCF#L# gene 56 neurofibromatosis 56 static encephalopathy 56 biochemical imbalance 56 familial adenomatous polyposis 56 FGFR2 gene 56 Li Fraumeni 56 Raynaud syndrome 56 Comorbid 56 bronchopulmonary dysplasia 56 autosomal dominant inheritance 56 puerperal psychosis 56 Polycystic Ovarian Syndrome 56 Inflammatory Bowel 56 ostomy surgery 56 neuro musculoskeletal 56 Acute Respiratory Failure 56 Wilms Tumor 56 Sleep disordered breathing 56 Bronchiectasis 56 facioscapulohumeral muscular dystrophy 56 Polycystic kidney disease 56 craniofacial deformities 56 lymphangioleiomyomatosis LAM 56 noninvasive painless 56 Sleep Disordered Breathing 56 lacunar 56 epigenetic changes 56 IL#R 56 hormonal abnormalities 56 meningitis encephalitis 56 autistic enterocolitis 56 neurologic complications 56 familial ALS 56 Dengue Shock 56 paragangliomas 56 von Willebrand 56 congenital cataract 56 Chronic ITP 56 Non Alcoholic Fatty 56 pyelonephritis 56 autistics 56 adrenal function 56 savant syndrome 56 developmental abnormalities 56 Chlamydia pneumoniae 56 CNTNAP2 56 Arnold Chiari 56 lumbar disc disease 56 Morquio Syndrome 56 shortened telomeres 56 neuroblastoma tumor 56 predisposing factor 56 APOE e4 56 neurologic disorders 56 gastric carcinoma 56 hyper IgE syndrome 56 Beta thalassemia 56 Sturge Weber syndrome 56 Pathological Gambling 56 Rheumatic Fever 56 imperfecta 56 brachial plexus palsy 56 diffuse intrinsic pontine glioma 56 Alopecia Areata 56 multi infarct dementia 56 atherothrombotic disease 56 molecular abnormalities 56 primary biliary cirrhosis 56 arterial calcification 56 hyperplastic 56 Tuberous Sclerosis Complex 56 collagen vascular 56 Loeys Dietz syndrome 56 facial clefts 56 Beckwith Wiedemann Syndrome 56 craniosynostosis 56 Osteosarcoma 56 Rett syndrome neurological disorder 56 fibrodysplasia ossificans progressiva 56 Peritoneal mesothelioma 56 thyroiditis 56 gastroesophageal reflux GERD 56 Hydrocephalus 56 colostomy ileostomy 56 vesicoureteral reflux VUR 56 biochemical imbalances 56 basal cell nevus syndrome 56 Periodontal disease 56 disorder thalassemia 56 bowel polyps 56 autistic spectrum 56 Systemic lupus erythematosus SLE 56 ALI ARDS 56 familial hypercholesterolemia 56 Neurological disorders 56 Duchene muscular dystrophy 56 psychiatric comorbidity 56 haemolytic uraemic syndrome 56 myasthenia gravis neuromuscular 56 Sclerosing 56 hydrops 56 Primary Immune Deficiency 56 axillary node 56 autistic regression 56 ORMDL3 56 hypophosphatasia 56 heterotaxy 56 microencephaly 56 clinicopathologic 56 cryptogenic 56 nonmelanoma skin cancers 56 aortic calcification 56 hepatorenal syndrome 56 Porphyria 56 obstructive sleep 56 bicuspid valve 56 Hemolytic uremic syndrome 56 asymptomatic PAD 56 attention-deficit/hyperactivity disorder ADHD 56 atopic disorders 56 comorbid ADHD 56 nephrogenic 56 fibrocystic 56 dyscalculia 56 Prader Willi syndrome 56 neurodevelopment disorders 56 metabolic abnormality 56 Prenatal Alcohol 56 Eclampsia 56 Acute Stress Disorder 56 overt hypothyroidism 56 Frontal lobe 56 Hirschsprung Disease 56 Obstructive Sleep Apnoea 56 autoinflammatory 56 cognitive dysfunctions 56 juvenile dermatomyositis 56 Idiopathic 56 proliferative diabetic retinopathy 56 Smith Magenis syndrome 56 Vitamin D insufficiency 56 Autism Spectrum Disorders 56 pseudotumor cerebri 56 mastocytosis 56 hyperparathyroidism 56 unprovoked seizures 56 WDR# 56 Patellofemoral 56 Hip dysplasia 56 post natally 56 monoclonal gammopathy 56 erythema nodosum 56 2 diabetes T2D 56 nerve palsy 56 Acute Myelogenous Leukemia 56 placenta praevia 56 invasive ductal breast cancer 56 Alzheimers disease 56 Lewy Body Dementia 56 Polymorphic Ventricular Tachycardia CPVT 56 #q#.# [001] 56 dermatomyositis 56 chromosome #p#.# 56 nonpsychiatric 56 Pleural Mesothelioma 56 immunodeficiency 56 channelopathies 56 carcinoid tumors 56 osteogenesis imperfecta 56 CMV infection 56 TTR amyloidosis 56 Undiagnosed 56 Irlen Syndrome 56 highly heritable 56 Parkinson disease multiple sclerosis 56 craniofacial anomalies 56 vulvodynia 56 gastrointestinal malignancies 56 cranio 56 BPS IC 56 Parkinsons disease 56 Alzheimer Disease AD 55 rheumatoid arthritis lupus 55 1 Antitrypsin Deficiency 55 Crouzon Syndrome 55 perinatal mood 55 chromosomal deletions 55 intraventricular hemorrhage 55 carcinoid tumor 55 cytomegalovirus infection 55 synaptic function 55 atopic eczema 55 systemic mastocytosis 55 gait disturbance 55 Sensory Integration Disorder 55 JMML 55 Congenital Heart Disease 55 microvascular dysfunction 55 Hurler Syndrome 55 Antisocial Personality Disorder 55 periodontal infection 55 Interstitial Cystitis 55 Prosopagnosia 55 diabetic retinopathy DR 55 severe congenital neutropenia 55 Hypophosphatasia 55 Sporadic CJD 55 microsatellite instability 55 paralysis blindness 55 syndromic 55 polyarticular 55 neuroblastomas 55 Wilms Tumour 55 chronic granulomatous disease 55 neurocognitive disorder 55 dimentia 55 Irritable bowel syndrome 55 Urinary tract 55 Venous thromboembolism 55 autism cerebral palsy 55 upper airway obstruction 55 Niemann Pick Disease 55 Fanconi 55 fetal chromosomal 55 Lennox Gastaut Syndrome 55 bladder dysfunction 55 autistic traits 55 petit mal seizures 55 SNHL