Related by context. All words. (Click for frequent words.) 73 chromosome abnormality 70 dominantly inherited 70 chromosomal defect 70 Dravet syndrome 69 rare chromosomal disorder 69 Holoprosencephaly 69 transfusion syndrome 69 CHD7 69 Beckwith Wiedemann syndrome 68 MCAD deficiency 68 ectodermal dysplasia 68 Apert syndrome 68 myelomeningocele 68 chromosomal disorder 68 congenital disorders 68 medium chain acyl 68 cerebellar hypoplasia 68 Angelman syndrome 68 Cockayne syndrome 68 Spinal muscular atrophy 67 skeletal dysplasia 67 mosaicism 67 Hutchinson Gilford progeria 67 Spina bifida 67 dyskeratosis congenita 67 Joubert syndrome 67 Hurler syndrome 67 autosomal recessive 67 genetic syndromes 67 Severe Combined Immunodeficiency 67 aneuploidies 67 hydrops 67 de novo mutations 67 twin transfusion 67 myotonic dystrophy 67 monogenic 67 DiGeorge syndrome 67 anencephaly 67 gene MECP2 67 choriocarcinoma 67 recessively inherited 67 congenital diaphragmatic hernia 66 pseudotumor cerebri 66 polyhydramnios 66 osteogenesis imperfecta 66 genetic abnormality 66 teratoma 66 dysgenesis 66 inherited mutations 66 uterus didelphys 66 lissencephaly 66 brain malformation 66 neurofibromas 66 Leber congenital amaurosis 66 galactosemia 66 microdeletion 66 DiGeorge Syndrome 66 chromosomal anomaly 66 diaphragmatic hernia 66 Medulloblastoma 66 Hirschsprung disease 66 congenital anomaly 65 Noonan Syndrome 65 inherited neurological disorder 65 carcinoid tumor 65 embryonal rhabdomyosarcoma 65 fibromatosis 65 Brugada Syndrome 65 ANCA associated 65 polydactylism 65 pyloric stenosis 65 Anencephaly 65 Arnold Chiari Malformation 65 Myocarditis 65 Crouzon Syndrome 65 CHARGE syndrome 65 chromosome abnormalities 65 immunodeficiency disorder 65 hereditary deafness 65 blastoma 65 chromosomal anomalies 65 congenital disorder 65 Hashimoto thyroiditis 65 persistent pulmonary hypertension 65 molar pregnancy 65 situs inversus 65 Fanconi anemia 65 recessive inheritance 65 fronto temporal dementia 65 aplasia 65 VCFS 65 phthalate syndrome 65 neurodevelopmental disorder 65 developmental abnormalities 65 recessive trait 65 Ectopia Cordis 64 incurable genetic 64 thyroid hormone deficiency 64 hemophagocytic lymphohistiocytosis 64 Crouzon syndrome 64 dermoid cyst 64 hydrocephaly 64 Chiari malformation 64 leukoencephalopathy 64 biliary atresia 64 neurodegenerative disorder 64 autosomal dominant disorder 64 chromosomal disorders 64 Lafora disease 64 autosomal recessive genetic 64 hamartoma 64 microchimerism 64 deafness neurological 64 leukodystrophy 64 HGPS 64 IgA deficiency 64 fibrous dysplasia 64 FMR1 gene 64 hypertrophic cardiomyopathy HCM 64 ADPKD 64 hereditary spastic paraplegia 64 Li Fraumeni syndrome 64 WAGR syndrome 64 autosomal dominant 64 congenital anomalies 64 neurofibroma 64 ARVD 64 Hypoplastic Left Heart 64 systemic amyloidosis 64 nonhereditary 64 inherited retinal degeneration 64 hypoplasia 63 chromosomal abnormality 63 fibroma 63 Eisenmenger syndrome 63 Retinoblastoma 63 mental retardation epilepsy 63 variable immunodeficiency 63 Wegener granulomatosis 63 static encephalopathy 63 Wilm tumor 63 Alport Syndrome 63 HELLP 63 cystic fibrosis Duchenne muscular 63 spontaneous miscarriages 63 Retinopathy 63 MPGN 63 primary ciliary dyskinesia 63 Henoch purpura 63 neurodevelopment disorder 63 autosomal dominant polycystic kidney 63 osteopetrosis 63 ependymoma 63 Sandhoff disease 63 Wolf Hirschhorn 63 degenerative disorder 63 chromosome #q#.# [001] 63 polydactyly 63 polycystic 63 congenital hypothyroidism 63 systemic scleroderma 63 #q# deletion 63 Chiari Malformation 63 Usher Syndrome 63 chorioamnionitis 63 chronic granulomatous disease 63 achromatopsia 63 brain lesions 63 Ebstein anomaly 63 herpesviruses 63 Langerhans cell histiocytosis 63 Hirschsprung Disease 63 ataxia telangiectasia 63 pre cancerous lesion 63 herpes simplex encephalitis 63 cortical dysplasia 63 syringomyelia 63 atresia 63 myelogenous leukemia 63 Fragile X Syndrome 63 paraganglioma 63 paraneoplastic 63 Folic acid deficiency 63 Alport syndrome 63 hypertrophic obstructive cardiomyopathy 63 von Hippel Lindau 63 leiomyomas 63 biliary atresia rare 63 neuropsychiatric disorder 63 FXTAS 63 ectopia cordis 63 malformation 63 Klinefelter syndrome 62 prenatally diagnosed 62 mental retardation blindness 62 Von Willebrand disease 62 pulmonary metastasis 62 toxemia 62 granule cells 62 G#S mutation 62 Endometrial cancer 62 immunodeficiencies 62 hyperplastic 62 progressive neurodegenerative disorder 62 somatic mutation 62 autosomal recessive disorder 62 primitive neuroectodermal tumors 62 hyperinsulinism 62 Marfan Syndrome 62 #q#.# deletion syndrome 62 Crigler Najjar syndrome 62 Dysplasia 62 congenital deafness 62 NF2 62 Meckel Gruber 62 MCADD 62 Becker muscular dystrophy 62 NF1 62 necrotizing enterocolitis 62 incurable neurological disorder 62 hypoplastic 62 Hutchinson Gilford Progeria Syndrome 62 peripartum cardiomyopathy 62 Morquio syndrome 62 auditory neuropathy 62 medulloblastoma tumors 62 sCJD 62 hamartomas 62 post transplant lymphoproliferative 62 limb deformities 62 Hip dysplasia 62 Rh factor 62 fatal neurodegenerative 62 diffuse intrinsic pontine glioma 62 Usher syndrome 62 motor neuron degeneration 62 mastocytosis 62 heart syndrome HLHS 62 dystrophy 62 meningeal 62 Pelizaeus Merzbacher disease 62 cortical blindness 62 genetic disorder 62 angiosarcoma 62 retinal dysfunction 62 degenerative neurological disorder 62 cerebri 62 neuroblastoma tumor 62 Polycystic ovary syndrome 62 Neurofibromatosis type 62 congenital cataract 62 lichen planus 62 hepatoblastoma 62 metabolic disorder 62 polycystic kidneys 62 autoimmune encephalitis 62 monozygotic twin 62 ectopic 62 Beta thalassemia 62 fetal malformations 62 leptin deficiency 62 undiagnosed celiac disease 62 spastic diplegia 62 bicuspid valve 62 Kufs disease 62 CHDs 62 congenital abnormalities 62 MECP2 gene 62 roseola 62 hemolytic disease 62 infection progressive multifocal 62 enterocolitis 62 autosomal recessive disease 62 Krabbe Leukodystrophy 62 discoid lupus 62 Wiskott Aldrich Syndrome 62 pancreatic endocrine 62 Ehlers Danlos syndrome 62 hypopituitarism 62 recurrent laryngeal nerve 62 Fanconi Anemia 62 supratentorial 61 Alagille syndrome 61 genetically inherited 61 PNET 61 Fragile X gene 61 skeletal malformations 61 Moyamoya disease 61 mitochondrial disorders 61 Childhood Disorder 61 Leber hereditary optic neuropathy 61 MC4R gene 61 NPHP 61 cystic fibrosis chronic pancreatitis 61 thyroiditis 61 arthrogryposis 61 pulmonary hypoplasia 61 septo optic dysplasia 61 alveolar rhabdomyosarcoma 61 optic nerve hypoplasia 61 congenital adrenal hyperplasia CAH 61 Eclampsia 61 progressive multifocal PML 61 nerve degeneration 61 placenta praevia 61 Vitamin B# deficiency 61 Aicardi syndrome 61 Phenylketonuria PKU 61 retinal dystrophy 61 heterotaxy 61 Rett syndrome 61 neurological abnormalities 61 subdural bleeding 61 chronic autoimmune disorder 61 Cryptococcus neoformans 61 DIPG 61 fatal neuromuscular disorder 61 synovial sarcoma 61 chromosome deletion 61 multisystem disease 61 gastric carcinoma 61 recessive genetic 61 chromosome rearrangements 61 degenerative neurological disease 61 Joubert Syndrome 61 pulmonary atresia 61 neurofibromatosis type 61 multisystem disorder 61 diabetes insipidus 61 familial adenomatous polyposis FAP 61 Niemann Pick disease 61 Osteogenesis imperfecta 61 omphalocele 61 JAK mutations 61 malformations 61 genetic defect 61 truncus arteriosus 61 normal karyotype 61 clefting 61 spastic paraplegia 61 histiocytosis 61 Sanfilippo Syndrome 61 neonatal lupus 61 neurologic deficits 61 rhabdomyosarcoma 61 MELAS 61 Proteus syndrome 61 lysosomal storage disease 61 skeletal abnormalities 61 Retinitis pigmentosa 61 bladder exstrophy 61 hyperemesis 61 encephalitis swelling 61 Meckel Gruber syndrome 61 neurological dysfunction 61 Polycystic ovary syndrome PCOS 61 #p#.# [001] 61 Wilms tumor 61 spongiform encephalopathies 61 pre eclamptic 61 Myasthenia gravis 61 JMML 61 tricuspid atresia 61 achondroplasia 61 Pulmonary hypertension 61 Muscular dystrophy 61 otosclerosis 61 Hutchinson Gilford Progeria 61 paralysis blindness 61 superior mesenteric artery 61 fatal neurodegenerative disorder 61 Hurler Syndrome 61 Long QT Syndrome 61 recurrent miscarriages 61 enteroviral infection 61 Hurthle cell 61 polycystic ovary syndrome PCOS 61 mitochondrial dysfunction 61 Rh incompatibility 61 preeclamptic 61 neuro degenerative disease 61 frontotemporal dementia 61 spinocerebellar ataxia 61 amniotic fluid embolism 61 Glioblastoma Multiforme GBM 61 atrioventricular septal defect 61 RPE# 61 Tuberous sclerosis 61 polycystic ovary syndrome 61 neuroblastomas 61 neural tube defect 61 Wiskott Aldrich syndrome 61 Six3 61 acute myocarditis 61 Meningiomas 61 filaggrin 61 Pervasive Developmental Disorder 60 Hyperthyroidism 60 inherited neurodegenerative 60 encephalitis meningitis 60 untreated celiac disease 60 Cysts 60 aniridia 60 hypotonia 60 Beckwith Wiedemann Syndrome 60 Bardet Biedl syndrome 60 congenital birth defects 60 immunocompetent 60 myopathies 60 Sporadic CJD 60 polymyalgia rheumatica 60 Prion diseases 60 infantile hemangioma 60 behavioral abnormalities 60 cystic kidney 60 orchitis 60 embryonal 60 Rhabdomyosarcoma 60 malignant transformation 60 sporadic Creutzfeldt Jakob 60 neonatal encephalopathy 60 juvenile dermatomyositis 60 HELLP syndrome 60 APOL1 60 Neisseria 60 antiphospholipid syndrome 60 Raynaud disease 60 agenesis 60 Persistent Pulmonary Hypertension 60 ataxias 60 autoimmune thyroiditis 60 egg follicles 60 hydatid disease 60 Epstein Barr Virus 60 lymphangioleiomyomatosis LAM 60 genetic imprinting 60 Goldenhar syndrome 60 immunodeficiency 60 uterine tumors 60 esophageal atresia 60 blood clotting disorder 60 GPC5 60 immuno deficiency 60 Metastases 60 epidermolysis bullosa 60 PPCM 60 neurocysticercosis 60 epidermolysis bullosa EB 60 congenital blindness 60 toxocariasis 60 hemolytic 60 metachromatic leukodystrophy 60 Hemangiomas 60 Myopathy 60 gastroschisis 60 progressive neurodegenerative 60 ependymomas 60 genes predisposing 60 hereditary disorders 60 Brugada syndrome 60 microcephalin 60 periventricular 60 severe aplastic anemia 60 Stargardt Macular Dystrophy 60 corpus luteum 60 beta thalassemia 60 hereditary blindness 60 subdural haemorrhage 60 herpes viruses 60 KRAS oncogene 60 brachial plexus palsy 60 FTLD 60 progressive degeneration 60 chromosomal imbalance 60 bicuspid aortic valve 60 dissociative disorders 60 gastrointestinal dysfunction 60 Leber Congenital Amaurosis LCA 60 bronchopulmonary dysplasia 60 idiopathic pulmonary 60 Ehrlichiosis 60 intraventricular hemorrhage 60 genetic neuromuscular disorder 60 lactase deficiency 60 Hemolytic Uremic Syndrome HUS 60 microcephaly 60 pigmentosa 60 fetu 60 cardiac tamponade 60 Radiographic findings 60 maternally inherited 60 glomerulonephritis 60 Krabbe Disease 60 juvenile myelomonocytic leukemia 60 dilated cardiomyopathy 60 tuberous sclerosis complex 60 familial ALS 60 neuritic 60 abnormal chromosomes 60 lymphoblastic lymphoma 60 trophoblastic 60 encephalitis inflammation 60 thymoma 60 chromosomal deletions 60 Cushing syndrome 60 clotting disorder 60 intractable epilepsy 60 DiGeorge syndrome rare 60 varicella infection 60 prosopagnosia 60 TEL AML1 60 optic atrophy 60 MELAS syndrome 60 IUGR 60 Gestational diabetes 60 neuro degenerative 60 GISTs 60 gene APOE4 60 microfilariae 60 hereditary disorder 60 HMGA2 60 Lou Gehrigs disease 60 hemorrhagic colitis 60 Leber congenital amaurosis LCA 60 primordia 60 incurable degenerative 60 podocytes 60 neuroligins 60 genetic abnormalities 60 incurable neurodegenerative disease 60 Hypertrophic 60 epilepsies 60 congential 60 multiorgan 60 LVNC 60 Rubinstein Taybi syndrome 60 alpha thalassemia 60 polycystic ovarian syndrome PCOS 60 Combined Immune Deficiency 60 Prox1 60 aneuploid cells 60 Newborn screening 60 Niemann Pick 60 nerve palsy 60 bullous 60 arrhythmogenic right 60 thrombophilia 59 autoinflammatory diseases 59 demyelinating disease 59 Epidermolysis bullosa 59 Epstein Barr virus EBV 59 neurogenetic 59 fibrodysplasia ossificans progressiva FOP 59 generalized epilepsy 59 Genetic predisposition 59 nephrosis 59 infarcts 59 Diabetic neuropathy 59 ductal breast cancer 59 exocrine 59 cysticercosis 59 retinal degeneration 59 Angelman 59 myotonic muscular dystrophy 59 Arrhythmogenic Right Ventricular Cardiomyopathy 59 Intussusception 59 Congenital Adrenal Hyperplasia 59 Wilms Tumor 59 dysmorphic features 59 causative gene 59 Pre eclampsia 59 neurofibrillary 59 smoldering myeloma 59 monozygotic twins 59 Septicemia 59 G6PD deficiency 59 necrotizing 59 nephronophthisis 59 MYH9 gene 59 stem glioma 59 maple syrup urine 59 craniofacial defects 59 Prader Willi syndrome 59 inflammatory demyelinating 59 congenita 59 Long QT syndrome 59 Cerebral palsy 59 sirenomelia 59 #q#.# [002] 59 polymyalgia 59 autistic regression 59 lysosomal diseases 59 SHANK3 59 meningitis encephalitis 59 neuro developmental disorder 59 IRS1 59 bone deformities 59 chromosomal defects 59 aneuploidy 59 mtDNA mutations 59 basal cell nevus syndrome 59 Hypophosphatasia 59 SCA1 59 Systemic lupus erythematosus 59 neurologic symptoms 59 muscle degeneration 59 chromosomal alterations 59 BARD1 59 imperfecta 59 prematurity ROP 59 mitochondrial disease 59 inheritable genetic 59 bronchogenic carcinoma 59 Parasitic twins 59 dysphasia 59 esophageal reflux 59 spinal muscular atrophy SMA 59 osteosarcomas 59 combined immunodeficiency SCID 59 Congenital 59 chronic idiopathic 59 HbF 59 Ribavirin causes 59 Borrelia 59 Urinary tract 59 epigenetic changes 59 progranulin mutations 59 Mycoplasma pneumoniae 59 abnormal chromosome 59 neuro degenerative disorder 59 extramedullary 59 cerebellar ataxia 59 neurological complications 59 myelodysplasia 59 congenital abnormality 59 endocrine tumors 59 myomas 59 incidentalomas 59 Polycystic kidney disease 59 diagnosed prenatally 59 thoracic aortic disease 59 polymorphic ventricular tachycardia 59 ambiguous genitalia 59 placenta accreta 59 Polycystic Ovary Syndrome 59 anterior temporal 59 lysosomal storage diseases 59 LRRK2 gene 59 CNTNAP2 59 thoracic aortic aneurysm 59 Neurofibromatosis Type 59 necrotizing enterocolitis NEC 59 severe congenital neutropenia 59 transplanted bone marrow 59 Papillary 59 necrotizing pneumonia 59 precancerous cervical 59 RDEB 59 chiari malformation 59 Treacher Collins syndrome 59 #q#.# [001] 59 neurological disorder affecting 59 TTTS 59 congenital scoliosis 59 skeletal deformities 59 Aplastic anemia 59 CMV infections 59 neuroblastoma tumors 59 autoimmune hemolytic anemia 59 β thalassemia 59 missense mutations 59 CFTR gene 59 Iron deficiency anemia 59 necrotising enterocolitis 59 dysautonomia 59 HMPV 59 Jakob Disease 59 aphthous stomatitis 59 Cystic fibrosis CF 59 intracerebral 59 Osteogenesis Imperfecta 59 chromosomal aberrations 59 Lesch Nyhan syndrome 59 Biliary atresia 59 adrenal cortex 59 leiomyoma 59 cholestasis 59 metabolic acidosis 59 Aortic stenosis 59 associated tremor ataxia 59 anatomical abnormalities 59 nonalcoholic cirrhosis 59 microdeletions 59 Sanfilippo syndrome 59 VHL gene 59 eosinophilic 59 adenomyosis 59 familial adenomatous polyposis 59 Leukemias 59 thyroid dysfunction 59 placental insufficiency 59 Malformations 59 infantile hemangiomas 59 intrauterine infection 59 Diffuse Intrinsic Pontine Glioma 59 oligodendrogliomas 59 MYCN amplification 59 Myotonic dystrophy 59 Bacterial vaginosis 59 frontotemporal 59 Guillain Barré Syndrome 59 Systemic lupus erythematosus SLE 59 necrotising 59 FMR1 59 congenital deformity 59 xeroderma pigmentosum 59 Toxoplasmosis 59 polycystic disease 59 oral thrush 59 enteroviral 59 epigenetic alterations 59 Coeliac disease 59 unexplained infertility 59 Creutzfeld Jakob disease 59 exocrine glands 59 mesenteric 59 CMV infection 59 Cockayne Syndrome 59 craniopagus parasiticus 59 predisposing factor 59 HNPCC 59 spine curvature 59 primitive neuroectodermal tumor 59 proliferative retinopathy 59 spinal bifida 59 enzyme deficiency 59 cisplatin resistant 59 MeCP2 gene 59 Fatty liver 59 cystic fibrosis muscular dystrophy 59 epigenetic modification 59 Irritable bowel syndrome IBS 59 Tay Sachs Disease 59 microvascular disease 58 bacterium Neisseria meningitidis 58 Dilated cardiomyopathy 58 neural tube 58 periventricular leukomalacia 58 Cholangiocarcinoma 58 herpes encephalitis 58 seizures comas 58 Genetic mutation 58 Trichomonas 58 Kabuki syndrome 58 cryptogenic 58 Dwarfism 58 recessive dystrophic epidermolysis bullosa 58 Legg Calvé Perthes disease 58 TCF#L# gene 58 WDR# 58 neuro developmental disorders 58 profound deafness 58 toxoplasmosis 58 congenital muscular dystrophy 58 reproductive endocrine 58 LHON 58 HHV 6 58 carcinoid 58 testicular tumors 58 Pervasive Developmental Disorders 58 malignant hyperthermia 58 C1q 58 abnormalities 58 mitochondrial diseases 58 pancreatic tissue 58 SMN protein 58 primordial germ cells 58 1 diabetes T1D 58 neurologic complications 58 retinitis pigmentosa RP 58 myositis 58 Gorlin syndrome 58 genetic alteration 58 insulin secreting 58 premature ovarian 58 systemic mastocytosis 58 polycystic ovarian disease 58 pituitary tumors 58 Osteosarcoma 58 Biliary Atresia 58 acute viral infection 58 Sclerosing 58 nephrogenic 58 hypoxic ischemic encephalopathy 58 benign polyps 58 epididymitis 58 premalignant 58 chromosomal rearrangement 58 huntingtin gene 58 metabolic abnormality 58 neurosensory 58 hemolytic anemia 58 pancytopenia 58 MEF2A 58 myeloproliferative 58 neurona 58 MeCP2 protein 58 motor neuron diseases 58 ischemic colitis 58 CDH1 58 leukoencephalopathy PML 58 mitochondrial mutations 58 dengue hemorrhagic fever DHF 58 cytomegalovirus infection 58 phenylketonuria 58 TTR amyloidosis 58 haemochromatosis 58 mesothelial cells 58 patent ductus arteriosus 58 BCL#A 58 nodular lesions 58 genetic lysosomal storage 58 mice lacking 58 myelin insulation 58 idiopathic epilepsy 58 nongenetic 58 gastrointestinal stromal tumor 58 congenital glaucoma 58 Moraxella catarrhalis 58 Marfan 58 Sjögren syndrome 58 myelopathy 58 kernicterus 58 Duchenne muscular dystrophy DMD 58 Mitochondrial disease 58 placental abruption 58 arthrogryposis multiplex congenita 58 Kawasaki Disease 58 p# mutations 58 intracranial hemorrhage bleeding 58 PTPN# 58 Moebius syndrome 58 vWD 58 imprinted genes 58 Polycystic Ovarian Syndrome PCOS 58 meningoencephalitis 58 trophoblasts 58 rare autosomal recessive 58 mucus glands 58 AAT deficiency 58 Wernicke Korsakoff syndrome 58 HLA B# 58 germline mutations 58 Smith Lemli Opitz syndrome 58 GIST tumors 58 tumoral 58 congenital brain tumor 58 motor neuropathy 58 microvessels 58 ceroid lipofuscinosis NCL 58 demyelinating 58 NR#A# 58 channelopathies 58 Viral infections 58 polycystic ovaries 58 hematological abnormalities 58 hormonal abnormalities 58 osteogenesis imperfecta OI 58 perinatal asphyxia 58 stress cardiomyopathy 58 Malformation 58 Ets2 58 TP# mutation 58 degenerative neurological condition 58 Loeys Dietz syndrome 58 tics involuntary 58 Celiac sprue 58 papillary carcinoma 58 TSC1 58 Ewing sarcoma bone 58 T1DM 58 hereditary predisposition 58 hypoplastic left 58 corneal epithelial 58 kyphosis 58 eosinophilic esophagitis 58 multiforme 58 erythema nodosum 58 hormonal disorder 58 kidney urologic 58 missense mutation 58 fetal chromosomal 58 vasa previa 58 acute lymphoid leukemia 58 Treacher Collins 58 haematopoietic 58 ventricular septum 58 congenital malformations 58 MC1R 58 ovarian malignancy 58 fatal myelination disorder 58 Pompe Disease 58 congenital adrenal hyperplasia 58 DICER1 58 induced cardiomyopathy 58 Autoimmune disorders 58 KCNE2 58 sonographic diagnosis 58 causative genes 58 velo cardio facial 58 breast carcinomas 58 petit mal seizures 58 Genital herpes 58 CNTNAP2 gene 58 glutamic acid decarboxylase 58 mitochondrial myopathy 58 precocious puberty 58 narcolepsy cataplexy 58 PCOD 58 lymphoblastic leukemia 58 blastomeres 58 subventricular zone 58 Parkinson degenerative 58 abnormal hemoglobin 58 coagulopathy 58 LRAT 58 fibrous tangles 58 cardiac fibrosis 58 Plasmodium parasites 58 cerebro spinal fluid 58 somatic mutations 58 Malignant mesothelioma 58 Nephrogenic Systemic Fibrosis NSF 58 Glioblastoma multiforme GBM 58 congenital insensitivity 58 maternally transmitted 58 ectoderm 58 Folate deficiency 58 sacral agenesis 58 cryptococcal meningitis 58 #p#.# [002] 58 PANDAS 58 kidney insufficiency 58 arterial calcification 58 postnatally 58 cultured neurons 58 enterovirus infection 58 Klinefelter Syndrome 58 Purkinje cells 58 Menkes disease 58 Chronic fatigue 58 pituitary adenoma 58 BRAF gene 58 respiratory gastrointestinal 58 teratomas 58 Cowden syndrome 58 de ath 58 susceptibility gene 58 lymphocytic 58 plexiform 58 chronic lymphocytic 58 CCR5 delta# 58 synaptogenesis 58 Glioma 58 Trichophyton rubrum 58 dysplasias 58 pulmonary thromboembolism 58 intracellular bacteria 58 hereditary nonpolyposis colorectal cancer 58 Leber Hereditary Optic Neuropathy 58 retinitis pigmentosa degenerative 58 NOTCH1 58 Peutz Jeghers syndrome 58 Moebius Syndrome 58 neurological sequelae 58 cardiomyopathy 58 pilocytic astrocytoma 58 LIS1 58 sickle hemoglobin 58 autoinflammatory 58 spontaneous mutation 57 benign growths 57 radial glia 57 degenerative retinal disease 57 bacterium Mycobacterium tuberculosis 57 lipomas 57 fetal microchimerism 57 overt hypothyroidism 57 idiopathic PAH 57 Hereditary angioedema 57 Reactive Attachment Disorder 57 Ectodermal Dysplasia 57 R#W [002] 57 abnormal prions 57 torticollis 57 hematologic disorders 57 PTEN gene 57 involuntary tics 57 Perthes disease