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(Click for frequent words.) 78 abnormality 73 malformations 69 developmental abnormalities 68 chromosomal abnormalities 68 abnormal 68 neurological abnormalities 67 congenital malformations 67 congenital anomalies 67 aneuploidies 65 congenital abnormalities 65 structural abnormalities 65 hydrops 64 Abnormalities 64 hamartomas 64 calcifications 64 malformation 64 hamartoma 64 biochemical abnormalities 63 cardiac abnormalities 63 genetic abnormalities 63 brain lesions 63 anatomical abnormalities 63 physiological abnormalities 63 neurologic symptoms 63 lesions 63 clefting 62 chromosome abnormalities 62 hyperplastic 62 abnormal growths 62 testicular tumors 62 genetic abnormality 62 microbleeds 61 genetic defects 61 inherited mutations 61 lung lesions 61 chromosomal anomalies 61 dysmorphic features 61 de novo mutations 61 chromosomal aberrations 61 thyroid nodules 61 chromosomal disorders 61 chromosomal defects 60 thyroid dysfunction 60 behavioral abnormalities 60 neurosensory 60 genetic syndromes 60 Hip dysplasia 60 genetic defect 60 perfusion defects 60 hypoplasia 60 chromosomal anomaly 60 hydronephrosis 60 polyhydramnios 60 benign growths 60 subclinical 60 da mage 60 myopathies 60 infarcts 60 microcalcifications 59 morphological abnormalities 59 hereditary predisposition 59 mosaicism 59 nonischemic 59 neurologic abnormalities 59 motor neuron degeneration 59 cognitive deficits 59 neurocognitive deficits 59 LVNC 59 GBA mutations 59 white matter hyperintensities 59 chromosomal alterations 59 brain malformation 59 malperfusion 59 chromosomal abnormality 59 congenital cataract 59 precancerous polyp 59 heterotaxy 59 abnormal heartbeats 59 sonographic examination 59 nerve degeneration 59 disorders 59 neurologic deficits 58 thyroid abnormalities 58 congenital malformation 58 holoprosencephaly 58 congenital anomaly 58 metabolic abnormality 58 diaphragmatic hernia 58 autosomal dominant inheritance 58 subclinical atherosclerosis 58 nerve palsy 58 neoplasms 58 somatic mutations 58 LRRK2 mutations 58 cortical thinning 58 epigenetic changes 58 leiomyomas 58 mitral stenosis 58 metabolic abnormalities 58 deformities 58 myelomeningocele 58 microdeletion 58 genital abnormalities 58 gene mutations 58 situs inversus 58 dysgenesis 58 chromosome abnormality 58 SNHL 58 sonographic findings 58 radiographic findings 58 incidentalomas 58 microdeletions 58 subclinical hyperthyroidism 58 atherosclerotic lesions 58 aortic regurgitation 58 neurofibromas 58 recurrent miscarriages 58 parkinsonism 58 chromosomal rearrangement 58 long QT syndrome 58 untreated celiac disease 57 congenital hypothyroidism 57 vascular dysfunction 57 vascular abnormalities 57 fusiform 57 sonographic diagnosis 57 cardiomyopathies 57 genetic mutations 57 adenomatous polyps 57 ovarian hormones 57 ectopic 57 chromosomal disorder 57 exotropia 57 haematuria 57 carcinoid tumor 57 anterior temporal 57 meniscal tears 57 IUGR 57 transfusion syndrome 57 retinal hemorrhages 57 Brugada syndrome 57 mitochondrial dysfunction 57 adenomas 57 congenital disorders 57 IgA deficiency 57 dystrophies 57 amyloid deposits 57 MCAD deficiency 57 dysplastic 57 arthrography 57 calculi 57 microvascular disease 57 autistic traits 57 vesicoureteral reflux 57 fetal malformations 57 carotid stenosis 57 chromosomal defect 57 pyloric stenosis 57 malignant polyps 57 chromosome aberrations 57 hypopituitarism 57 neurodevelopmental disorder 57 ECG abnormalities 57 Hashimoto thyroiditis 57 intraoperative complications 57 hippocampal function 57 bone deformities 57 ADPKD 57 Cushing syndrome 57 dysplasia 57 adenoma 57 hyperreflexia 56 breast lesions 56 amyloid deposition 56 egg follicles 56 nephrogenic 56 germline mutations 56 noncardiac 56 pituitary tumors 56 microvessels 56 NP CRNs 56 mucosal lesions 56 persistent pulmonary hypertension 56 tumoral 56 microscopic hematuria 56 mutations 56 lipomas 56 pathophysiologic 56 osteochondromas 56 echogenicity 56 syndromes 56 symptoms 56 hypertrophic cardiomyopathy HCM 56 recurrent laryngeal nerve 56 achromatopsia 56 mental retardation epilepsy 56 proliferative diabetic retinopathy 56 ovarian malignancy 56 bullous pemphigoid 56 Plaque buildup 56 underwent coronary angiography 56 angiographically 56 congenital abnormality 56 subclinical hypothyroidism 56 hematuria 56 normal karyotype 56 neurological degeneration 56 thyroiditis 56 pre malignant lesions 56 defects 56 cerebellar vermis 56 autonomic dysfunction 56 cholestasis 56 MECP2 gene 56 hypoperfusion 56 nodular lesions 56 thyroid hormone levels 56 ovarian cysts 56 hippocampal atrophy 56 granule cells 56 neoplasias 56 computerized tomography scans 56 acetabular dysplasia 56 artery stenosis 56 congenital defects 56 thrombi 56 Klinefelter syndrome 56 endometrial cancers 56 sporadic ALS 56 amenorrhoea 56 lissencephaly 56 pituitary adenomas 56 atypical hyperplasia 56 pathologic fractures 56 retinal detachment 56 periventricular 56 subcortical 56 elevated liver enzymes 56 Genetic variants 56 vascular cognitive impairment 56 DCIS lesions 56 oculomotor 56 cerebellar 56 obstructive coronary artery 56 neurocognitive impairments 56 CHD7 56 malignant transformation 56 prognostic significance 56 ipRGCs 56 ARVD 56 cardiomegaly 56 cognitive impairment 56 APOE e4 56 enamel defects 56 nodal metastases 55 atypia 55 cysts 55 ganglion cysts 55 nonmelanoma skin cancers 55 postoperative complication 55 retinopathy 55 leptin deficiency 55 guinea pigs lubiprostone 55 familial clustering 55 Hemangiomas 55 urolithiasis 55 laterality 55 papilledema 55 parathyroid 55 gliosis 55 Ultrasound scans 55 hyperinsulinism 55 skeletal malformations 55 lymphatic tissue 55 vascularity 55 perfusion abnormalities 55 hyperparathyroidism 55 neuronal dysfunction 55 thyroid nodule 55 vessel occlusion 55 hirsutism 55 meningiomas 55 hypoplastic 55 defects CHDs 55 malignancies 55 JAK mutations 55 pulmonary hypoplasia 55 pelvic ultrasound 55 chromosome #q#.# [001] 55 familial ALS 55 neurological symptoms 55 cervical lymph nodes 55 myocardial ischemia 55 sensorineural hearing loss 55 ovarian tumors 55 neurologic complications 55 pleural effusions 55 neuropathologic 55 de ath 55 DNA methylation patterns 55 Malignant tumors 55 Sjögren syndrome 55 prostate abnormalities 55 occipital lobes 55 chromosome rearrangements 55 craniofacial anomalies 55 polycystic ovary syndrome PCOS 55 neuromotor 55 enterocolitis 55 pilocytic astrocytomas 55 denervation 55 Ebstein anomaly 55 precursor lesions 55 nevi 55 neurological complications 55 genetic mutations Spoor 55 histologic examination 55 arterial calcification 55 gastric carcinoma 55 intestinal polyps 55 pathologic diagnosis 55 anatomic abnormalities 55 adrenal masses 55 CMV infections 55 Cancerous cells 55 cystic lesions 55 thyroid hormone deficiency 55 polydactyly 55 SRBD 55 cardiac tamponade 55 sCJD 55 cardiac fibrosis 55 histopathologic 55 sonographic appearance 55 prenatally diagnosed 55 paragangliomas 55 poorer prognosis 55 thoracic aortic aneurysm 55 proximal colon 55 thyrotoxicosis 55 pituitary adenoma 55 vestibular schwannomas 55 synaptic function 55 varicoceles 55 pathologies 55 primary ciliary dyskinesia 55 pre cancerous lesion 55 osteosarcomas 55 LQTS 55 neurodevelopmental outcome 55 seminomas 55 FXTAS 55 neuropsychological impairments 55 supratentorial 55 familial adenomatous polyposis 55 #q# deletion 55 autosomal dominant disorder 55 bowel cancers 55 predisposing factor 55 ventricular enlargement 55 lymphadenopathy 55 fetal aneuploidy 55 vestibular dysfunction 55 hormonal abnormalities 55 gene variants 55 Microscopic examination 55 myometrium 55 mesotheliomas 55 MGUS 55 GISTs 55 neural tube defect 55 HLHS 55 teratoma 55 colorectal polyps 55 carotid plaques 55 developmental delays 55 hypotonia 55 schwannomas 55 S#A# [002] 55 osteochondroma 55 subclinical disease 55 NAFLD 55 diagnosed prenatally 55 acute aortic dissection 54 utero exposure 54 mtDNA mutations 54 Retinopathy 54 Coronary artery calcium 54 meningeal 54 metabolic disturbances 54 enlarged ventricles 54 cardioembolic stroke 54 malignant tissues 54 hemolytic disease 54 biochemical markers 54 epithelial tissues 54 repolarization 54 systemic amyloidosis 54 cortical blindness 54 schwannoma 54 pericardial effusions 54 reproductive abnormalities 54 predisposing factors 54 polyomavirus nephropathy 54 sonographically 54 hemangiomas 54 kidney insufficiency 54 histopathologic examination 54 hyperplastic polyps 54 retinal dysfunction 54 fibrocystic 54 pathogenic mutations 54 benign breast 54 fronto temporal dementia 54 dopamine transporter gene 54 atresia 54 p# mutations 54 osteochondrosis 54 deformational plagiocephaly 54 Histopathologic examination 54 carotid artery stenosis 54 mitochondrial mutations 54 chromosomal deletions 54 bleedings 54 neurodevelopmental disorders 54 perioperative complications 54 genetic polymorphisms 54 chromosomal instability 54 labral tears 54 trisomy 54 neurocognitive impairment 54 neurologic 54 hardened arteries 54 untreated sleep apnea 54 glaucomatous 54 motor neuropathy 54 Colon polyps 54 parahippocampal gyrus 54 posterior fossa 54 limb deformities 54 endometrial hyperplasia 54 idiopathic 54 premalignant lesions 54 ultrasonographic 54 HbF 54 chorioamnionitis 54 atrophic 54 hypertrophic obstructive cardiomyopathy 54 leukoencephalopathy 54 enterovirus infection 54 rCBF 54 desmin 54 Beckwith Wiedemann syndrome 54 ependymomas 54 pre cancerous growths 54 anovulation 54 adnexal mass 54 progressive degeneration 54 neuritic 54 Adenomas 54 malignant lesions 54 electrical conduction 54 varicocele 54 benign lesions 54 SCN5A 54 molar pregnancy 54 spine curvature 54 arterial occlusion 54 #q#.# [002] 54 gene rearrangements 54 painless lump 54 recurrent miscarriage 54 arrhythmogenic right 54 alkalosis 54 arteriogram 54 BRCA1 mutations 54 benign polyps 54 pulmonary emboli 54 precancerous tumors 54 fibrous dysplasia 54 neoplastic lesions 54 amblyopia lazy eye 54 invasive carcinoma 54 placental tissues 54 cryptorchidism 54 neurological sequelae 54 menstrual abnormalities 54 cardiac hypertrophy 54 hypoxemia 54 paraneoplastic 54 subdural haemorrhage 54 cardiac dysfunction 54 impair fertility 54 polycystic kidneys 54 trophoblasts 54 reflux disease 54 coronary artery stenosis 54 dysregulation 54 atrioventricular 54 epigenetic alterations 54 arrhythmias 54 PTEN mutations 54 bowel polyps 54 lymphangioleiomyomatosis LAM 54 uveal melanoma 54 colorectal neoplasms 54 fatty infiltration 54 neuropathological 54 sensory receptors 54 cerebral infarction 54 C. pneumoniae 54 aniridia 54 fibroma 54 Cowden syndrome 54 epididymitis 54 hypometabolism 54 necrotizing 54 deformity 54 torsade de pointes 54 abnormal rhythms 54 adrenal function 54 mammographically 54 carotid artery ultrasound 54 azoospermia 54 neoplasm 54 prolonged QT interval 54 pulmonary vasculature 54 endocrine abnormalities 54 metabolic derangements 54 thromboses 54 artery blockages 54 VUR 54 hyperintensity 54 transesophageal echocardiography 54 transcranial Doppler 54 neuroimaging studies 54 Metastases 54 silent myocardial ischemia 54 activated microglia 54 cerebral arteries 54 troponin T 54 skeletal abnormalities 54 facial clefts 54 subthalamic 54 advanced adenoma 54 cortical atrophy 54 Doppler sonography 54 advanced adenomas 54 Apert syndrome 54 craniofacial defects 54 cytopenia 54 G6PD deficiency 54 myocyte 54 underlying pathophysiology 54 gait abnormalities 54 pathologic 54 lung nodules 54 diastolic dysfunction 54 morphologic 54 clinically detectable 54 aortic atherosclerosis 54 etiologic 54 thyroid carcinoma 53 refractive error 53 neuropsychiatric disorder 53 hematopoietic cancers 53 ductal carcinomas 53 cerebral vasospasm 53 microglial 53 carotid atherosclerosis 53 electrophysiologic 53 malignant nodules 53 Fetal heartbeats 53 chromosomal imbalance 53 skeletal deformities 53 Charcot foot 53 pancreatic endocrine 53 polyps 53 Graves ophthalmopathy 53 adrenal hyperplasia 53 retinal vascular 53 penetrance 53 infantile hemangiomas 53 computed tomography scans 53 bladder cancers 53 genetic mutation 53 CHDs 53 catheter angiography 53 pulmonary toxicity 53 renal cell carcinomas 53 extrapyramidal symptoms 53 molecular abnormalities 53 mucinous 53 chromosomal rearrangements 53 calcium buildup 53 oesophageal 53 hypokalemia hypomagnesemia 53 subconjunctival hemorrhage 53 ataxias 53 renal artery stenosis 53 primary ovarian insufficiency 53 conjunctivitis pink 53 Heavy menstrual bleeding 53 synovial 53 eosinophilia 53 atherosclerotic lesion 53 mesenteric 53 drusen 53 ZNF# 53 anatomic structures 53 preterm deliveries 53 temporoparietal 53 metastases 53 dysplasias 53 cancerous lesion 53 interstitial fibrosis 53 phenotype 53 embryonic tissues 53 artery occlusion 53 habitual snoring 53 phthalate syndrome 53 inherited predisposition 53 ventricular dysfunction 53 hypermethylated 53 radiographically 53 infarctions 53 nystagmus 53 KCNH2 53 neuro developmental disorders 53 histopathological 53 polymorphic ventricular tachycardia 53 bullous 53 nonobstructive 53 arrhythmogenic 53 myocardial fibrosis 53 cataract formation 53 Eisenmenger syndrome 53 renal scarring 53 nuchal 53 malignant tumors 53 pathognomonic 53 coronary artery dissection 53 basilar 53 pulmonary nodules 53 lymph node metastases 53 stratifying patients 53 intraparietal sulcus 53 coarctation 53 dominantly inherited 53 pAkt 53 deep vein thromboses 53 hyperactivation 53 extracolonic findings 53 coronary blockages 53 proliferative retinopathy 53 androgen excess 53 bronchopulmonary dysplasia 53 cerebral cortical 53 urethral stricture 53 highly heritable 53 fetal chromosomal 53 tricuspid atresia 53 fetal anomalies 53 pre cancerous lesions 53 Cysts 53 multisystem disease 53 mutant huntingtin protein 53 Radiographs 53 arteriography 53 HGPS 53 hyperinsulinemia 53 bladder dysfunction 53 axillary lymph nodes 53 asymptomatic 53 neuroblastomas 53 cancerous polyps 53 monogenic 53 microfractures 53 troponins 53 abnormal vaginal bleeding 53 metastatic lesions 53 thyroid function 53 fibroadenoma 53 brain infarcts 53 phthalate exposure 53 neurodevelopmental outcomes 53 neuropathies 53 hypercalciuria 53 myopia nearsightedness 53 bicuspid aortic valves 53 paraganglioma 53 choroidal neovascularization CNV 53 epigenetic markers 53 posterior vitreous detachment 53 chest radiography 53 adenoid 53 methylation patterns 53 colorectal adenomas 53 NF1 53 orchitis 53 mammillary bodies 53 Doppler imaging 53 chromosomal translocations 53 ventricular septal defects 53 pre cancerous 53 retinal nerve 53 mammary cancers 53 preeclamptic 53 dysplastic lesions 53 oxygen saturations 53 BRCA1 BRCA2 53 leiomyoma 53 prefrontal regions 53 N myc 53 cardiac troponin 53 Asymptomatic 53 gastric distention 53 lymph node enlargement 53 prenatal ultrasound 53 breast abscesses 53 diplopia 53 frontotemporal 53 adrenal cortex 53 rhythm disturbances 53 lymph node metastasis 53 obstructive coronary 53 oral clefts 53 adrenocortical cancer 53 dysmotility 53 detect abnormalities 53 serotonin transporters 53 olfactory dysfunction 53 Lewy bodies 53 postnatally 53 APOE ε4 53 abnormal chromosomes 53 Arrhythmogenic Right Ventricular Cardiomyopathy 53 Idiopathic 53 bladder tumors 53 HER2 amplification 53 aortic coarctation 53 cortical activation 53 CIN2 + 53 monoclonal gammopathy 53 #.#ng/ml 53 benign positional vertigo 53 prion infection 53 otosclerosis 53 lobular breast cancer 53 bicuspid aortic valve 53 Doppler echocardiography 53 phonic tics 53 hyperbilirubinemia 53 cryptogenic 53 intestinal metaplasia 53 beta1 integrin 53 endometrioid 53 genetic polymorphism 53 transvaginal sonography 53 serotonin defects 53 cognitive impairments 53 plasma kallikrein 53 genomic rearrangements 53 susceptibility genes 53 plain radiographs 53 thymectomy 53 synaptogenesis 53 affective psychoses 53 genetic variations 53 abnormal genital 53 lichen planus 53 histological 53 pheochromocytoma 53 clinically insignificant 53 heterotopic ossification 53 glomerulonephritis 53 genetic determinants 53 underactive thyroid gland 53 QTc prolongation 53 mediastinum 53 BRCA2 gene 53 histone modifications 53 haemorrhages 53 metabolic acidosis 53 Iron deficiency anemia 53 Wernicke encephalopathy 53 jugular venous 53 breast endometrial 53 varicella infection 53 anencephaly 53 ASDs 52 Vitamin B# deficiency 52 Hemorrhagic strokes 52 lysosomal diseases 52 alveolar bone loss 52 CHEK2 52 histological examination 52 microalbuminuria 52 immunodeficiencies 52 brachial plexus palsy 52 atypical moles 52 metabolic dysfunction 52 cancerous lesions 52 seroma 52 thyroid cancers 52 coronary stenosis 52 hyperexcitability 52 polyps growths 52 melanocytic 52 microvascular dysfunction 52 POAG 52 optic nerve sheath 52 scintigraphy 52 noncancerous 52 pituitary hormone 52 parenchymal 52 CDH# 52 biochemical imbalances 52 medial temporal 52 Multivariate analyzes 52 histologically 52 malignant prostate 52 TMPRSS2 ERG fusion 52 neoplastic cells 52 hyperplasia 52 microvascular complications 52 nodules 52 genetically inherited 52 folic acid deficiency 52 sentinel nodes 52 LIS1 52 kyphosis 52 gyri 52 peri implant 52 parathyroid gland 52 sleep disturbances 52 stenoses 52 brain parenchyma 52 ascertainment bias 52 lumbosacral 52 mutant genes 52 somatosensory cortex 52 intrauterine infection 52 motoneurons 52 sonographic examinations 52 micro calcifications 52 pericardial effusion 52 cecal 52 Arteriovenous Malformation 52 mammary cells 52 psychiatric disorders 52 carotid artery blockage 52 GATA4 52 airway hyperresponsiveness 52 heterozygotes 52 postoperative delirium 52 Leydig cell 52 genetic aberrations 52 FDG uptake 52 FGFR2 gene 52 periventricular leukomalacia 52 ultrastructural 52 genetic alterations 52 Computed tomography 52 Loeys Dietz syndrome 52 abnormal lipid 52 Malformations 52 overactivity 52 hemiparesis 52 MYCN amplification 52 neurological 52 coronary stenoses 52 disordered breathing 52 vasogenic edema 52 valvular heart disease 52 fundus photography 52 Hyperthyroidism 52 Intussusception 52 irregular menstrual periods 52 otitis 52 SMAD4 52 thyrotropin levels 52 polypoid lesions 52 pathologic examination 52 Dysplasia 52 chest radiographs 52 ectoderm 52 osteoblastic 52 erythema nodosum 52 neurofibroma 52 EBV infection 52 echocardiographic 52 microcephaly 52 pre eclamptic 52 impaired cognition 52 WDR# 52 edematous 52 polycystic ovarian syndrome PCOS 52 iritis 52 periodontal infections 52 Li Fraumeni syndrome 52 intracerebral 52 Torsades de Pointes 52 left ventricular hypertrophy 52 ductal 52 AAT deficiency 52 connexin 52 cancerous lumps 52 cytogenetic abnormalities 52 hypervascular 52 neurosyphilis 52 T2 weighted images 52 geometric distortions 52 Lyme arthritis 52 carcinomatosis 52 TP# mutations 52 corpus luteum 52 thermogram 52 septal defects 52 chromosomal aberration 52 microsatellite instability 52 oxygen desaturation 52 ambiguous genitalia 52 vascular anomalies 52 histopathological examination 52 teratogens 52 Wernicke Korsakoff syndrome 52 fetal echocardiogram 52 nonhereditary 52 Ultrasonography 52 dizygotic twins 52 malignant neoplasm 52 Doppler ultrasonography 52 congenital glaucoma 52 precancerous condition 52 estrogen deficiency 52 congenital disorder 52 tricuspid regurgitation 52 autopsied brains 52 gallstone disease 52 myeloperoxidase 52 Aortic valve 52 hyperhomocysteinemia 52 encephalitis inflammation 52 ventral 52 macrovascular complications 52 mesothelial cells 52 cytologic 52 placental malaria 52 DEXA scans 52 giant cell arteritis 52 EKG electrocardiogram 52 dentinal hypersensitivity 52 agenesis 52 trigeminal ganglia 52 hyperintensities 52 cerebral angiography 52 chorionic villi 52 Hurthle cell 52 autistic tendencies 52 Sonographic 52 electrolyte abnormalities 52 spontaneous mutation 52 opacities 52 intima media thickness 52 ischemic lesions 52 advanced neoplasia 52 benign proliferative breast 52 fibrosis 52 lymphocytic 52 lymphatics 52 nasal obstruction 52 fetal chromosomal abnormalities 52 sinus node dysfunction 52 thyroid stimulating hormone 52 amnestic MCI 52 lymphatic vasculature 52 uterine bleeding 52 deafness meningitis 52 cognitive dysfunction 52 enzyme elevations 52 histologic 52 Multivariate analysis 52 tumors 52 distant metastasis 52 Chest x rays 52 aneuploidy 52 neurologic disorders 52 ductal adenocarcinoma 52 cytogenic 52 prostate carcinogenesis 52 comorbidities 52 Long QT syndrome 52 anterior uveitis 52 nonvascular 52 paresis 52 aortic rupture 52 uterus womb 52 ICD shocks