Related by context. All words. (Click for frequent words.) 82 autosomal recessive 75 autosomal dominant disorder 73 autosomal recessive disorder 69 inherited neurological disorder 69 progressive neurodegenerative disorder 68 dominantly inherited 67 idiopathic 67 familial ALS 67 NF1 67 sporadic ALS 67 paraneoplastic 67 fatal neurodegenerative 67 monogenic 67 autosomal recessive disease 66 IgA deficiency 66 autosomal recessive genetic 66 dyskeratosis congenita 66 neurodegenerative disorder 66 neuropsychiatric disorder 66 Li Fraumeni syndrome 65 myeloproliferative 65 autosomal 65 inherited neurodegenerative 65 tuberous sclerosis complex 65 proband 65 ADPKD 65 tics involuntary 65 de novo mutations 65 essential thrombocythemia 65 infantile onset 65 nonhereditary 65 missense mutation 65 ataxias 65 progressive degeneration 64 inherited mutations 64 fatal neurodegenerative disorder 64 Cervical dystonia 64 Leber congenital amaurosis 64 FTLD 64 Retinitis Pigmentosa RP 64 dysgenesis 64 MELAS 64 Hutchinson Gilford progeria 64 systemic amyloidosis 64 heterozygous 64 mosaicism 64 MECP2 gene 64 neurofibromatosis type 64 Tuberous sclerosis 64 Angelman syndrome 64 HNPCC 64 Hashimoto thyroiditis 64 lysosomal storage disease 64 incurable neurodegenerative disease 64 holoprosencephaly 64 RPE# 64 ANCA associated 63 Cockayne syndrome 63 CDH1 63 genetically inherited 63 germline mutations 63 neurofibromas 63 gene MECP2 63 situs inversus 63 glomerulonephritis 63 neurological manifestations 63 primary ciliary dyskinesia 63 motor neuron degeneration 63 Sydenham chorea 63 autosomal dominant inheritance 63 MLH1 63 C#Y 63 recessive trait 63 MYH9 gene 63 methylenetetrahydrofolate reductase 63 HGPS 63 MTHFR 63 idiopathic PAH 63 vWD 63 supratentorial 63 Bardet Biedl syndrome 63 paraganglioma 63 apolipoprotein E gene 63 heterozygotes 63 phenotype 63 hypogonadotropic hypogonadism 63 erythematosus 63 myotonic dystrophy 63 progressive neurodegenerative 62 immunodeficiencies 62 demyelinating 62 Wolf Hirschhorn 62 Upregulation 62 hereditary hemochromatosis 62 huntingtin gene 62 Aortic stenosis 62 Wiskott Aldrich syndrome 62 Sjögren syndrome 62 homozygous 62 genetic abnormality 62 enteropathy 62 von Willebrand disease 62 congenital adrenal hyperplasia CAH 62 recessive inheritance 62 neoplasm 62 PTPN# 62 AAT Deficiency 62 LRAT 62 demyelination 62 xeroderma pigmentosum 62 inherited retinal degeneration 62 spinocerebellar ataxia type 62 homozygous familial hypercholesterolemia 62 GISTs 62 SMN1 62 microdeletion 62 leiomyomas 62 missense mutations 62 SSc 62 idiopathic generalized epilepsy 62 penetrance 62 hereditary hemorrhagic telangiectasia 62 chromosome abnormality 62 frontotemporal dementia 62 hypoplasia 62 Von Willebrand disease 62 Cowden syndrome 62 Pervasive Developmental Disorder 62 Leber congenital amaurosis LCA 62 familial hypercholesterolemia 62 homozygosity 62 hereditary disorder 62 chromosome #q#.# [001] 62 HLA B# 62 MLL gene 62 hyperplastic 62 Alport syndrome 62 congenital disorders 61 Homozygous 61 5q 61 pheochromocytoma 61 Myotonic dystrophy 61 Brugada Syndrome 61 recessive genetic 61 aplasia 61 familial adenomatous polyposis 61 hepatocellular carcinomas 61 Leydig cell 61 euthymic patients 61 Hereditary angioedema HAE 61 #q#.# [001] 61 neurological disorder characterized 61 neurofibrillary 61 ectodermal dysplasia 61 spinocerebellar ataxia 61 frameshift mutation 61 polymyalgia rheumatica 61 nonsense mutation 61 WAGR syndrome 61 thyroiditis 61 apolipoprotein E APOE 61 fibrous dysplasia 61 endocrine disorder 61 cytogenetic abnormalities 61 Meckel Gruber syndrome 61 fungoides 61 allelic variants 61 normal karyotype 61 cell adhesion molecule 61 autoinflammatory diseases 61 chromosomal abnormality 61 Pulmonary hypertension 61 LHON 61 parkinsonism 61 Inflammatory bowel disease 61 glutamic acid decarboxylase 61 Polycystic ovary syndrome 61 osteochondroma 61 chronic eosinophilic leukemia 61 chromosome deletion 61 epididymitis 61 polydactyly 61 regulator CFTR gene 61 PAOD 61 systemic lupus erythematosus SLE 61 cutaneous lesions 61 Haptoglobin 61 Dysregulation 61 hereditary deafness 61 FXTAS 61 activating mutation 61 Sezary syndrome 61 Insulin resistance 61 diabetes mellitus DM 61 APOE gene 61 MODY 61 Childhood Disorder 61 ABCB1 61 Hypophosphatasia 61 neuronal dysfunction 61 immunodeficiency 61 enterocolitis 61 SCN5A 61 spontaneous mutation 61 Atopic dermatitis 61 Irritable bowel syndrome 61 JMML 60 Diabetic neuropathy 60 Peutz Jeghers syndrome 60 genetic defect 60 Diabetic nephropathy 60 Brugada syndrome 60 #q# [001] 60 beta thalassemia 60 Retinitis pigmentosa 60 nonsense mutations 60 Arrhythmogenic Right Ventricular Cardiomyopathy 60 mutated gene 60 missense 60 APOE e4 60 Holoprosencephaly 60 MGUS 60 severe congenital neutropenia 60 Spinal muscular atrophy 60 neurological disorder affecting 60 syngeneic 60 giant cell arteritis 60 histologic subtype 60 pathophysiologic 60 Niemann Pick disease 60 Meckel Gruber 60 neurologic disorder 60 sCJD 60 polymorphic ventricular tachycardia 60 lissencephaly 60 NF1 gene 60 multisystem disease 60 HLA DR4 immune 60 IL#R 60 Neurofibromatosis type 60 incomplete penetrance 60 chronic granulomatous disease 60 metaplasia 60 chromosome #q# [002] 60 Lupus nephritis 60 motor neuron diseases 60 breast carcinomas 60 Lafora disease 60 hyperparathyroidism 60 CC genotype 60 CFTR gene 60 myeloproliferative neoplasms 60 microsatellite instability 60 T2DM 60 Apolipoprotein E 60 mutation 60 #q#.# deletion syndrome 60 Medulloblastoma 60 familial hypercholesterolemia FH 60 Klinefelter syndrome 60 Psoriatic arthritis 60 microcephalin 60 NPM1 gene 60 mycosis fungoides 60 ADAMTS# 60 HFE gene 60 #q#.# [002] 60 #p#.# [002] 60 Cushing syndrome 60 CHD7 60 Hurler syndrome 60 decarboxylase 60 filaggrin 60 dystrophies 60 rs# [004] 60 1 diabetes T1D 60 autoimmune thyroid 60 c KIT 60 degenerative disorder 60 Mendelian 60 MSH2 60 paragangliomas 60 MC1R 60 rs# [002] 60 Essential tremor 60 causative gene 60 generalized tonic clonic seizures 60 polyposis 60 atypical hemolytic uremic syndrome 60 hyper IgE syndrome 60 pseudotumor cerebri 60 leukoencephalopathy 60 Becker muscular dystrophy 60 myeloid 60 inherited predisposition 60 Major depressive disorder 60 ependymoma 60 congenita 59 basal cell nevus syndrome 59 familial aggregation 59 Male pattern baldness 59 Gorlin syndrome 59 PNET 59 Retinopathy 59 Hemophilia B 59 neurological dysfunction 59 cone photoreceptors 59 susceptibility gene 59 congenital anomaly 59 transgenic mouse models 59 polygenic 59 Leber hereditary optic neuropathy 59 genetic lysosomal storage 59 myoclonus 59 downregulation 59 lysosomal storage diseases 59 R#W [002] 59 amnestic 59 constitutively active 59 maternally inherited 59 Maroteaux Lamy Syndrome 59 homozygous FH 59 inherited neurodegenerative disorder 59 sporadic Creutzfeldt Jakob 59 PTEN gene 59 homocystinuria 59 VUR 59 spastic diplegia 59 teratoma 59 CAG repeats 59 DQB1 * 59 cortical dysplasia 59 Epstein Barr virus EBV 59 Vascular dementia 59 proliferative retinopathy 59 herpesviruses 59 Systemic lupus erythematosus 59 atrophic gastritis 59 pheochromocytomas 59 FMR1 gene 59 Papillary 59 lymphocytic 59 genes predisposing 59 hydrops 59 Retinoblastoma 59 heterotaxy 59 Klippel Trenaunay Syndrome 59 hyperplasia 59 immunocompetent 59 neurodevelopmental disorder 59 systemic lupus erythematosus 59 Frontotemporal dementia 59 leiomyoma 59 chronic idiopathic 59 Osteogenesis imperfecta 59 Ribavirin causes 59 FSGS 59 Fragile X Syndrome 59 gastric carcinoma 59 genetic neuromuscular disorder 59 LQTS 59 5q chromosome 59 Allergic rhinitis 59 autoinflammatory 59 habitual snoring 59 Philadelphia Chromosome Positive 59 Polycystic kidney disease 59 AAT deficiency 59 #q# deletion syndrome 59 eosinophilic 59 Congenital 59 Tourette Syndrome TS 59 Hyperthyroidism 59 Idiopathic 59 generalized epilepsy 59 aniridia 59 colorectal carcinoma 59 Kabuki syndrome 59 C#BL/#J 59 monozygotic twins 59 Maroteaux Lamy syndrome 59 lacunar 59 Acute lymphoblastic leukemia 59 defective gene 59 SHANK3 59 germline mutation 59 heritable 59 Cholangiocarcinoma 59 bullous 59 myasthenia gravis MG 59 granulomatous 59 enzyme deficiency 59 abnormal chromosome 59 Polymorphic Ventricular Tachycardia CPVT 59 #q# deletion 59 nonischemic 59 atopic 59 GH deficiency 59 Neurofibromatosis Type 59 carcinoid tumor 59 Bacterial vaginosis 59 hereditary spastic paraplegia 59 thrombocytosis 59 Schizoaffective disorder 59 septo optic dysplasia 59 Dysplasia 59 anterior uveitis 59 rare autosomal recessive 59 recessive dystrophic epidermolysis bullosa 58 subtype 58 monozygotic twin 58 pyelonephritis 58 chromosomal deletions 58 chromosomal translocation 58 neuroendocrine 58 TSC1 58 optic atrophy 58 alternatively spliced 58 GSTT1 58 hypereosinophilic syndrome 58 hyperinsulinism 58 Myasthenia gravis 58 acute myeloid 58 chronicity 58 T1DM 58 unmutated 58 hypopituitarism 58 retinitis pigmentosa RP 58 Coeliac disease 58 alleles 58 epilepsies 58 bexarotene 58 Severe Combined Immunodeficiency 58 mutant gene 58 sensory neuropathy 58 medium chain acyl 58 thymoma 58 hamartomas 58 non syndromic 58 Fanconi anemia 58 velo cardio facial 58 ataxia telangiectasia 58 basal cell carcinoma BCC 58 functional polymorphism 58 villous atrophy 58 amino acid substitution 58 mtDNA mutations 58 5 hydroxytryptamine 58 HLA DRB1 * 58 phenotypic expression 58 fatal neuromuscular disorder 58 TP# mutation 58 PDGFR 58 Trichophyton rubrum 58 Polycystic ovary syndrome PCOS 58 phenylketonuria 58 complement inhibitor eculizumab 58 myelofibrosis polycythemia vera 58 mGluR 58 capillary leak 58 primitive neuroectodermal tumors 58 neuro degenerative disease 58 immunodeficiency disorder 58 homozygotes 58 autoimmune thyroiditis 58 Obstructive sleep apnea 58 GNAQ 58 myopathies 58 clinically heterogeneous 58 SLC#A# [001] 58 incurable neurological disorder 58 nephritis 58 PON1 58 Malignant mesothelioma 58 Janus kinase 58 neuroblastomas 58 inherited genetic mutations 58 neovascular 58 pancytopenia 58 affective psychoses 58 Chronic lymphocytic leukemia 58 NAGS deficiency 58 COL#A# 58 karyotype 58 childhood disintegrative disorder 58 cause cardiac channelopathies 58 TTR amyloidosis 58 WNK1 58 progressive degenerative 58 chronic autoimmune disorder 58 leukemia AML 58 Dilated cardiomyopathy 58 PTEN mutations 58 gene polymorphism 58 von Hippel Lindau 58 osteogenesis imperfecta 58 HbF 58 constitutively expressed 58 common hematologic malignancy 58 promoter polymorphism 58 ApoE gene 58 homolog 58 recessive mutation 58 optic neuropathy 58 periventricular 58 malignant fibrous histiocytoma 58 heart valve insufficiency 58 hydroxylase 58 mutant allele 58 demyelinating disease 58 etiologic 58 recessive gene 58 recessively inherited 58 unknown etiology 58 demyelinating diseases 58 atresia 58 androgenetic alopecia 58 Joubert syndrome 58 Dravet syndrome 58 proliferative diabetic retinopathy 58 Leber Hereditary Optic Neuropathy 58 neurological abnormalities 58 Androgenetic alopecia 58 hyperalgesia 58 Leber Congenital Amaurosis LCA 58 blood clotting disorder 58 papillary RCC 58 G#S mutation 58 choroidal neovascularization 58 Basal cell carcinoma 58 sensorineural hearing loss 58 galactosemia 58 Angiotensin II 58 mediastinitis 58 Loeys Dietz syndrome 58 cerebellar 58 syringomyelia 58 chromosomal defect 58 Glioma 58 NF2 58 thrombophilia 58 Leukemias 58 Lymphocytic 58 relapsing remitting 58 variable immunodeficiency 58 #beta HSD1 58 premorbid 58 Six3 58 arrhythmogenic 58 axonal damage 58 Pulmonary arterial hypertension 58 pancreatic endocrine 58 Congenital Adrenal Hyperplasia 58 experimental autoimmune encephalomyelitis 58 maternally transmitted 58 thyrotoxicosis 58 tricuspid atresia 58 unprovoked seizures 57 VHL gene 57 Anaplastic 57 lymphoblasts 57 congenital deficiency 57 Beta thalassemia 57 Langerhans cell histiocytosis 57 retinal degeneration 57 survival motor neuron 57 myelopathy 57 thrombocytopenia neutropenia 57 mice lacking 57 renal fibrosis 57 fibroma 57 Nf1 57 metabolic abnormalities 57 infarcts 57 CCR5 delta# 57 pyloric stenosis 57 myelodysplastic syndrome MDS 57 chronic inflammatory bowel 57 juvenile myelomonocytic leukemia 57 dysmotility 57 CNTNAP2 57 vasculopathy 57 neurofibroma 57 G#S [002] 57 autosomal dominant polycystic kidney 57 Carcinoid tumors 57 haemolytic 57 cerebellar hypoplasia 57 ENPP1 57 neoplastic 57 Overexpression 57 V#F mutation 57 myelodysplasia 57 Cystic fibrosis CF 57 nonalcoholic steatohepatitis NASH 57 Spina bifida 57 TACI 57 adrenal insufficiency 57 plasminogen activator inhibitor 57 H#K# methylation 57 Chorea 57 neoplasias 57 Endometrial cancer 57 Diabetic retinopathy 57 myeloproliferative diseases 57 congenital adrenal hyperplasia 57 inherited maternally 57 somatic mutation 57 retinitis 57 cerebral vasospasm 57 Dystrophin 57 IL 1ß 57 erythema nodosum 57 agenesis 57 dystrophy 57 steatohepatitis 57 ceroid lipofuscinosis NCL 57 Oppositional Defiant Disorder 57 aldehyde dehydrogenase 57 evolutionarily conserved 57 CDKN2A 57 acute leukemias 57 neuropsychiatric disorders 57 schizoaffective disorder bipolar 57 G6PD deficiency 57 telomere dysfunction 57 #p#.# [001] 57 akinesia 57 APOC3 57 HNSCC 57 Ankylosing spondylitis 57 Gestational diabetes 57 inflammatory demyelinating 57 FMR1 57 humans variant Creutzfeldt 57 CIAS1 57 haplotype 57 polyneuropathy 57 proteolytic processing 57 disabling neurological 57 OPRM1 gene 57 nephronophthisis 57 systemic autoimmune 57 airway hyperresponsiveness 57 autoimmune hemolytic anemia 57 chromosomal rearrangement 57 Friedreich ataxia 57 heart syndrome HLHS 57 Parkinsonian 57 MYBPC3 57 Ehlers Danlos syndrome 57 Alleles 57 #p# [003] 57 Hutchinson Gilford Progeria Syndrome 57 receptor gene 57 ventricular myocardium 57 autoantibody positive 57 Epidermolysis bullosa 57 CYP#C# gene 57 subsyndromal 57 Fibrosis 57 transcriptional repressor 57 PALB2 57 Apert syndrome 57 hepatic lipase 57 mucinous 57 Stargardt Macular Dystrophy 57 gastrointestinal stromal tumor 57 superior mesenteric artery 57 fibrosing 57 papillary renal cell carcinoma 57 idiopathic thrombocytopenic purpura 57 Hemorrhagic 57 Sanfilippo Syndrome 57 Neuregulin 1 57 ischemic optic neuropathy 57 Peripheral neuropathy 57 post transplant lymphoproliferative 57 aneuploidy 57 Lennox Gastaut syndrome 57 KCNQ1 57 protein encoded 57 common disabling neurological 57 γ secretase 57 Renal cell carcinoma 57 generalized seizures 57 null mice 57 parkinsonian 57 beta globin 57 cytopathic 57 facioscapulohumeral muscular dystrophy 57 familial adenomatous polyposis FAP 57 subependymal giant cell 57 deletion 5q 57 Kufs disease 57 Cystic fibrosis 57 achondroplasia 57 Acute myeloid leukemia 57 Nf2 57 spontaneous mutations 57 chromosomal anomalies 57 LPS induced 57 debilitating autoimmune 57 imperfecta 57 metastatic malignant 57 Acute otitis media 57 proliferator activated receptor 57 APOL1 57 fibrosarcoma 57 nerve palsy 57 mutations 57 autonomic dysfunction 57 NPHP 57 monozygotic 57 asplenia 57 Parkinsonian Syndromes 57 choroidal neovascularization CNV 57 atopic asthma 57 orchitis 57 MTHFR gene 57 BH4 deficiency 57 prolonged QT interval 57 cystic fibrosis transmembrane conductance 57 Irritable bowel syndrome IBS 57 LIS1 57 hypercalcemia 57 independent prognostic marker 57 gene locus 57 diabetes mellitus T2DM 57 underlying vasculopathy 57 tumoral 57 multisystem disorder 57 phonic tics 57 osteopetrosis 57 acute myelogenous leukemia AML 57 urethritis 57 MALT lymphoma 57 Systemic lupus erythematosus SLE 57 Myelodysplastic syndromes 57 chronic myeloid 57 pathologic myopia 57 spastic paraplegia 57 monocytic 56 Asymptomatic 56 TP# mutations 56 achromatopsia 56 genetic mutation 56 ventricular fibrillation VF 56 ichthyosis 56 abnormal p# 56 dissociative disorders 56 muscarinic receptors 56 atopy 56 Usher syndrome 56 K ras mutations 56 presenilin 56 transgenic mice expressing 56 genomic variants 56 malignant neoplasm 56 predisposing factor 56 primary biliary cirrhosis 56 HBeAg negative 56 hereditary nonpolyposis colorectal cancer 56 distinct subtypes 56 Mitral regurgitation 56 long QT syndrome 56 NOTCH1 56 MEF2A 56 prion protein PrP 56 TACI mutations 56 highly heritable 56 DR4 56 osteosarcomas 56 KCNE2 56 leptin receptor 56 hyperprolactinemia 56 mediated apoptosis 56 NKX2 56 CFH gene 56 chromosomal disorder 56 synaptogenesis 56 HeFH 56 congenital abnormality 56 juvenile idiopathic arthritis JIA 56 hematologic disorders 56 allelic 56 intracytoplasmic 56 subclinical 56 T1D 56 Wernicke Korsakoff syndrome 56 PARP inhibition 56 Clusterin 56 APOE4 56 beta globin gene 56 paresis 56 primary generalized tonic 56 Chlamydia pneumoniae 56 aneuploidies 56 fibrotic disease 56 channelopathies 56 developmental abnormalities 56 TEAEs 56 gastric adenocarcinoma 56 Fas ligand 56 lichen planus 56 alpha1 56 neurodevelopment disorder 56 SMAD4 56 papillary thyroid carcinoma 56 Henoch purpura 56 hemolytic 56 acquired immunodeficiency syndrome 56 spasmodic torticollis 56 Bronchiectasis 56 Phosphorylation 56 tyrosine phosphorylation 56 cystic fibrosis chronic pancreatitis 56 nerve degeneration 56 CYP#C# [002] 56 Vitamin B# deficiency 56 NR#A# 56 frontotemporal dementia FTD 56 disorder ASD 56 lactose malabsorption 56 lupus erythematosus 56 epithelioid 56 incurable genetic 56 SCA5 56 Usher Syndrome 56 Beckwith Wiedemann syndrome 56 brain malformation 56 haematologic 56 hippocampal atrophy 56 degenerative retinal disease 56 intracerebral 56 ectopic expression 56 1α 56 multiple endocrine neoplasia 56 hypothalamic pituitary 56 Chronic lymphocytic leukemia CLL 56 ependymomas 56 pericardial effusion 56 JAK2 enzyme 56 paresthesias 56 gene mutation 56 mGluRs 56 paroxysmal nocturnal hemoglobinuria 56 cancerous enlargement 56 catenin 56 recurrent seizures 56 cystic fibrosis Duchenne muscular 56 Von Hippel Lindau 56 Fragile X gene 56 myelomeningocele 56 adenocarcinomas 56 Mendelian disorders 56 Congenital Muscular Dystrophy 56 neutropenia dehydration dyspnea 56 Heterozygous 56 carcinoids 56 eosinophilic esophagitis 56 Ischemic 56 epiglottitis 56 mitochondrial dysfunction 56 Hypertrophic 56 thyroid carcinoma 56 G allele 56 CD#b 56 dysregulated 56 Gleevec resistant 56 Purkinje cell 56 T2D 56 chronic neurological disorder 56 Hereditary angioedema 56 neurobiological disorder 56 Relapsing remitting MS 56 CD# CD# 56 vascular cognitive impairment 56 dopamine D4 receptor 56 Systemic lupus 56 optica 56 ductal adenocarcinoma 56 Hemangiomas 56 androgenic alopecia 56 HLA DR2 56 bulbar 56 erythematosus SLE 56 mood dysregulation 56 Rheumatoid arthritis RA 56 del 5q 56 Seborrheic dermatitis 56 Lesch Nyhan syndrome 56 underlying pathophysiology 56 genetic disorder 56 histologically 56 neurodegenerative disorder characterized 56 Osteosarcoma 56 Mucopolysaccharidosis 56 Idiopathic pulmonary fibrosis 56 LEOPARD syndrome 56 retinal blindness 56 GSTM1 56 Arrhythmogenic 56 ataxia 56 diabetes dyslipidemia 56 MLL2 56 Idiopathic pulmonary fibrosis IPF 56 chromosomal anomaly 56 Atopic eczema 56 Glucocorticoids 56 neuroligins 56 mental retardation epilepsy 56 iritis 56 Fanconi Anemia 56 BRAF gene 56 apolipoprotein E 56 poorer prognosis 56 medulloblastomas 56 muscular dystrophy cystic fibrosis 56 germline cells 56 trisomy 56 CTEPH 56 spinal muscle atrophy 56 elevated triglyceride levels 56 CHD5 56 cerebral infarction 56 SOD1 gene 56 Trigeminal neuralgia 56 dermatomyositis 56 sarcomatoid 56 lysosomal storage disorder 56 progressive retinal degenerative 56 Obsessive compulsive disorder 56 HMGA1 56 lymphocyte activation 56 mutated K ras 56 neural crest 56 non alcoholic steatohepatitis 56 endocannabinoid signaling 56 congenital anomalies 56 pathological hallmarks 56 coagulopathy 56 skeletal dysplasia 56 affective psychosis 56 dehydrogenase deficiency 56 transmembrane protein 56 lactase deficiency 56 alpha synuclein protein 56 RDEB 56 familial clustering 56 neuro developmental disorder 56 motoneurons 56 Wegener granulomatosis 56 T#I [002] 56 cholestasis 56 delayed gastric emptying 56 H#K#me# 56 pleomorphic 56 lysosomal 56 primary hyperoxaluria 56 purpura 56 Anencephaly 56 polyarticular 56 MELAS syndrome 56 DiGeorge syndrome 56 Myelodysplastic syndrome 56 mRNA expression 56 gastrointestinal stromal tumors GISTs 56 Thrombocytopenia 56 premalignant 56 Chronic pancreatitis 56 PsA 56 Fanconi anemia FA 56 SJIA 56 pRb 56 UGT#A# * 56 sustained ventricular tachycardia 56 debilitating neurodegenerative disorder 56 BCL#A 56 roseola 56 neonatal lupus 56 discoid lupus 56 transferase 56 neuronal degeneration 56 myeloproliferative disorder 56 transgene expression 56 retinal dysfunction 56 primitive neuroectodermal tumor 56 CNVs 56 neonatal respiratory distress 56 efferent 56 androgen receptor AR 56 Inappropriate activation 56 chromosomal aberrations 56 mito 56 comorbid anxiety 56 dystrophin gene 56 BRCA1 BRCA2 56 leukodystrophy