Related by context. All words. (Click for frequent words.) 79 mutated gene 73 genetic defect 73 mutant gene 72 genetic mutation 71 gene mutation 69 mutation 69 recessive gene 66 mutated genes 65 genetic abnormality 65 CFTR gene 65 BRCA2 gene 65 BRCA1 gene 65 abnormal hemoglobin 63 RPE# gene 63 RPE# 63 Fanconi anemia 62 genetic defects 62 genetic mutations 62 gene 62 ApoE4 gene 62 mutations 62 beta thalassemia 62 gene mutations 61 recessive mutations 61 G#S mutation 61 genetic disorder 61 recessive trait 61 genetic abnormalities 61 gene variant 61 mutant genes 61 chromosome abnormality 60 genetic variant 60 dystrophin gene 60 FMR1 gene 59 X chromosome 59 huntingtin gene 59 recessive genes 59 autosomal dominant 58 ApoE4 58 dystrophin 58 autosomal recessive disease 58 familial adenomatous polyposis 58 genetic trait 58 Joubert syndrome 58 hereditary disorder 58 genes predisposing 58 nonsense mutation 58 nonsense mutations 58 SMN1 gene 58 familial ALS 58 TP# mutation 58 SMN2 gene 58 PALB2 58 SMN protein 57 genes 57 APOE gene 57 NF1 57 MYH9 gene 57 myotonic dystrophy 57 mitochondrial dysfunction 57 autosomal recessive 57 SMN2 57 neural tube defect 57 APOE4 57 chromosomal abnormality 57 BRCA1 mutation 57 causative gene 57 BRCA mutation 57 Tay Sachs disease 57 SMN1 57 heterozygous 56 neurodegenerative disorder 56 homozygous 56 Leber congenital amaurosis 56 p# gene 56 C#Y 56 HNPCC 56 enzyme deficiency 56 gene variation 56 chromosomal disorder 56 MSH2 56 holoprosencephaly 56 inherited mutations 56 dyskeratosis congenita 56 APOE e4 56 susceptibility gene 56 chromosomal defect 56 Meckel Gruber 56 mutated protein 56 SORL1 56 LRAT 56 MECP2 gene 56 hemochromatosis 56 Dravet syndrome 56 PTEN gene 55 Lafora disease 55 faulty BRCA1 gene 55 tumor suppressor gene 55 CDH1 55 mutant protein 55 spontaneous mutations 55 genetic variation 55 apoE4 55 SHANK3 55 alleles 55 C1q 55 VHL gene 55 APOE4 gene 55 allele 55 Fragile X syndrome 55 mtDNA mutations 55 recessive mutation 55 BRIP1 55 CFTR protein 55 TACI mutations 55 chromosomal abnormalities 55 protein encoded 55 achromatopsia 55 Niemann Pick disease 55 mitochondrial disease 54 hereditary hemochromatosis 54 measles virus 54 MCAD deficiency 54 SOD1 gene 54 IgA deficiency 54 sporadic ALS 54 IGF2 54 chronic granulomatous disease 54 Kufs disease 54 congenital adrenal hyperplasia CAH 54 gene variants 54 hypertrophic cardiomyopathy HCM 54 Fragile X gene 54 X chromosomes 54 BRCA1 54 BRCA gene mutation 54 receptor protein 54 FTO gene 54 LQTS 54 HLA B# 54 mitochondrial diseases 54 BRCA1 mutations 54 galactosemia 54 degenerative disorder 54 MTHFR 54 autosomal dominant disorder 54 EGFR gene 54 dystrophin protein 54 recessive genetic 54 genetic variations 54 pneumococci 54 germline mutation 54 spontaneous mutation 54 MIF protein 54 mutated BRCA1 54 abnormal chromosome 54 APOE e4 gene 53 MIF gene 53 LMNA 53 de novo mutations 53 BCR ABL protein 53 autosomal recessive disorder 53 dominantly inherited 53 epigenetic changes 53 haemochromatosis 53 LRRK2 gene 53 prion disease 53 progranulin 53 BRAF gene 53 HFE gene 53 progranulin gene 53 abnormal prions 53 MTHFR gene 53 CNVs 53 inherited predisposition 53 Becker muscular dystrophy 53 BRCA gene 53 myostatin gene 53 LKB1 53 mosaicism 53 toxoplasmosis 53 BRCA2 53 ADPKD 53 aneuploidy 53 regulator CFTR gene 53 exfoliation glaucoma 53 AAT deficiency 53 LIS1 53 GSTT1 53 Six3 53 autoantibodies 53 NF1 gene 53 fatal neurodegenerative 53 retrovirus 53 genetic alteration 53 FXTAS 53 familial hypercholesterolemia 53 chromosome abnormalities 53 Rh positive 53 basal cell nevus syndrome 53 GFP gene 53 HMGA2 53 Wwox 53 CHD7 53 missense mutation 53 BRCA2 mutation 53 Klinefelter syndrome 53 RhD negative 52 protein dystrophin 52 parkin gene 52 cystic fibrosis transmembrane conductance 52 MC1R gene 52 brain malformation 52 phenylketonuria 52 Leber congenital amaurosis LCA 52 MLL gene 52 CHEK2 gene 52 Cockayne syndrome 52 pyloric stenosis 52 BRCA2 gene mutation 52 chromosomal aberrations 52 fetal hemoglobin 52 maternally inherited 52 Hashimoto thyroiditis 52 Angelman syndrome 52 IRAK1 52 SCN5A 52 metabolic disorder 52 Epstein Barr virus EBV 52 Hirschsprung disease 52 Peutz Jeghers syndrome 52 fronto temporal dementia 52 retinal degeneration 52 APOL1 52 WAGR syndrome 52 latent TB 52 Pdx1 52 breast cancer genes BRCA1 52 filaggrin 52 MCADD 52 Akt1 52 Beta thalassemia 52 apolipoprotein E gene 52 asymptomatically 52 genetically inherited 52 severe congenital neutropenia 52 polyomavirus nephropathy 52 varicella zoster virus 52 progerin 52 genetic predisposition 52 leptin deficiency 52 Von Willebrand disease 52 genetic variants 52 HLA genes 52 spinocerebellar ataxia 52 susceptibility genes 52 germline mutations 52 laforin 52 pseudotumor cerebri 52 Anencephaly 52 micro RNAs 52 familial adenomatous polyposis FAP 52 huntingtin protein 52 CNTNAP2 gene 52 degenerative neurological disorder 52 Friedreich ataxia 52 chromosomal alterations 52 cardiac channelopathies 52 medulloblastoma 52 HbF 51 primordial germ cells 51 hereditary deafness 51 sickle hemoglobin 51 ARVD 51 iron overload 51 TAp# 51 prion protein 51 GSTM1 gene 51 herpes infection 51 Li Fraumeni syndrome 51 COMT gene 51 recurrent miscarriages 51 Hurler syndrome 51 mutant allele 51 genetic alterations 51 HLA DQ2 51 genetic 51 enteroviruses 51 CAG repeats 51 Li Fraumeni 51 calcineurin 51 biliary atresia 51 mice lacking 51 defective mitochondria 51 myelomeningocele 51 Diamond Blackfan anemia 51 Brugada Syndrome 51 WT1 51 congenital disorder 51 ZNF# 51 penetrance 51 receptor molecule 51 RDEB 51 gamma globin gene 51 inherited neurological disorder 51 pneumococcal meningitis 51 neuroligins 51 p# mutations 51 IGF1 51 chromosome 51 PTEN mutation 51 lissencephaly 51 biochemical pathway 51 FMR1 51 abnormal chromosomes 51 SHANK3 gene 51 ApoE gene 51 globin 51 trisomy 51 androgen receptor gene 51 genetic disorders 51 FTLD 51 Noonan Syndrome 51 Fragile X Syndrome 51 Hutchinson Gilford progeria 51 YKL 51 transplanted bone marrow 51 Dystrophin 51 hereditary disorders 51 HGPS 51 TCF#L# gene 51 MC4R gene 51 progranulin protein 51 ovarian tumors 51 colon tumors 51 G#S [002] 51 haplotype 51 CCR5 mutation 51 HLA molecules 51 retinoblastoma 51 somatic mutations 51 Pompe Disease 51 gene p# 51 mammary cells 51 Foxp3 51 collagen VII 51 colon cancers 51 herpes virus 51 Runx1 51 Ets2 51 G#D mutation 51 5 HTT gene 51 genetically 50 FGFR2 50 OPRM1 gene 50 Skp2 50 myelodysplasia 50 Duchenne muscular dystrophy DMD 50 inherited genetic mutation 50 nestin 50 leptin resistance 50 Spinal muscular atrophy 50 congenital disorders 50 APOE 50 spinal muscle atrophy 50 congenital deafness 50 genes BRCA1 50 hydrops 50 Coeliac disease 50 TACI 50 Marfan syndrome 50 epigenetically 50 MC1R 50 polycystic ovary syndrome 50 asymptomatic carriers 50 pDCs 50 untreated celiac disease 50 fatal neuromuscular disorder 50 Cystic fibrosis 50 IKZF1 50 xeroderma pigmentosum 50 DICER1 gene 50 E4 variant 50 familial hypercholesterolaemia 50 mitochondrial mutations 50 protein fragment 50 KLF# 50 familial hypercholesterolaemia FH 50 heterotaxy 50 X SCID 50 F#del mutation 50 multisystem disease 50 mutant proteins 50 number variations CNVs 50 monogenic 50 genetic susceptibility 50 adenoma 50 filaggrin gene 50 hypertrophic cardiomyopathy 50 MeCP2 gene 50 Hemophilia B 50 endogenous retroviruses 50 Rett syndrome 50 genetically identical 50 GSTM1 50 Prox1 50 insulin secreting cells 50 Apert syndrome 50 DiGeorge syndrome 50 FMRP protein 50 type 1diabetes 50 TH# cells 50 leukaemic cells 50 STAT4 50 sCJD 50 epidermolysis bullosa EB 50 CCR5 delta# 50 podocytes 50 NFkB 50 glutamate signaling 50 UGT#B# 50 long QT syndrome 50 IL# [001] 50 DNA methylation patterns 50 thalassemia 50 chromosomal anomaly 50 FSGS 50 Heterozygous 50 klotho 50 abnormalities 50 transfusion syndrome 50 Rh factor 50 NF2 50 Fanconi Anemia 50 GBM tumors 50 epigenetic silencing 50 leptin receptors 50 placental function 50 Retinitis Pigmentosa RP 50 NEIL1 50 muscular dystrophies 50 DiGeorge Syndrome 50 causative genes 50 MECP2 50 BMPR2 50 gene APOE4 50 EBV infection 50 genetic markers 50 von Willebrand disease 50 mutant alleles 50 activating mutations 50 gene encoding 50 Wolbachia strains 50 familial pancreatic cancer 50 PALB2 gene 50 TSLP 50 bacterium E. coli 50 Wilms tumor 50 H. pylori 50 mutated BRCA 49 genetic syndromes 49 JAK2 mutation 49 PDGFRA 49 Loeys Dietz syndrome 49 GISTs 49 Brugada syndrome 49 thalassemia trait 49 neuroblastoma tumors 49 microcephalin 49 Helicobacter 49 beta globin 49 CNTNAP2 49 p# tumor suppressor 49 PTPN# 49 mutant mouse 49 beta globin gene 49 CHEK2 49 intestinal biopsy 49 apoE 49 NOTCH1 49 HLA G 49 ApoE 49 EZH2 49 progressive neurodegenerative disorder 49 Vitamin B# deficiency 49 homozygous FH 49 atherosclerotic lesions 49 Vpu 49 hereditary 49 MLH1 49 Bcr Abl 49 ChR2 49 microdeletions 49 latent TB infection 49 phenotype 49 herpes viruses 49 Tay Sachs 49 premature ovarian 49 teratoma 49 activin 49 abnormal growths 49 incurable genetic 49 breast cancer gene mutation 49 Neuregulin 1 49 pancreases 49 ApoE4 allele 49 chimeric mice 49 SOD2 gene 49 HLA B# gene 49 STK# gene 49 aY chromosome 49 polydactylism 49 bicuspid valve 49 Sanfilippo syndrome 49 inherited neurodegenerative disorder 49 hereditary diseases 49 TGFBR1 * 6A 49 SORL1 gene 49 nerve degeneration 49 Aplastic anemia 49 TP# gene 49 retinitis pigmentosa RP 49 TOMM# 49 medulloblastoma tumors 49 premutation 49 Bardet Biedl syndrome 49 fatty liver disease 49 Sandhoff disease 49 TB bacterium 49 SCA5 49 incurable neurodegenerative disease 49 vesicular stomatitis virus 49 Genetic mutations 49 pathogenic mutations 49 DICER1 49 miRNA genes 49 imprinted genes 49 transgenic mice 49 mitochondrial disorders 49 SLC#A# gene [001] 49 allelic variants 49 Fanconi Anaemia 49 mammalian embryos 49 disorder thalassemia 49 congenital hypothyroidism 49 neurofibromas 49 thoracic aortic aneurysm 49 amyloid plaque 49 PrP 49 normal prion proteins 49 Math1 49 polycystic ovarian syndrome PCOS 49 MODY 49 C EBP alpha 49 Alport syndrome 49 malignant transformation 49 Myotonic dystrophy 49 RUNX3 49 hereditary predisposition 49 endostatin 49 narcolepsy cataplexy 49 blood clotting disorder 49 lung adenocarcinoma 49 human leukocyte antigen 49 SOX3 gene 49 TEL AML1 49 Wolf Hirschhorn 49 INF2 49 gene MECP2 49 nonhereditary 49 herpesviruses 49 Beckwith Wiedemann syndrome 49 pancreatic tissue 49 GATA4 49 Klotho gene 49 pre eclampsia 49 fatal neurodegenerative disorder 49 cystic fibrosis Duchenne muscular 49 alpha synuclein gene 49 BRAF mutation 49 Smith Lemli Opitz 49 mutated K ras 49 polycystic ovary syndrome PCOS 49 MLL2 49 APOC3 49 chromosomal rearrangement 49 TNFa 49 AAV2 49 WDR# 49 somatic mutation 49 mice genetically engineered 49 Niemann Pick 49 HCMV 49 Fragile X 49 Sanfilippo Syndrome 49 DLX5 49 anaplastic lymphoma kinase 49 ataxia telangiectasia 49 biochemical signaling pathway 49 Cushing syndrome 49 cystic fibrosis 49 parainfluenza virus 49 antibodies 49 neuro degenerative disease 49 BRCA mutations 49 BRCA genes 49 Igf2 49 missense mutations 49 disease 49 DiGeorge syndrome rare 49 SLC#A# [001] 49 BMP2 49 BRCA2 breast cancer 49 CMV infection 49 spinal muscular atrophy SMA 49 blastomeres 49 lipin 49 BRCA2 mutations 49 microdeletion 49 cardiac hypertrophy 49 recessive inheritance 48 frontotemporal dementia 48 retinitis 48 Von Hippel Lindau 48 Y chromosome 48 asymptomatic 48 HLA matched 48 thyroid hormone 48 TCF4 48 UGT#A# * 48 neuroblastomas 48 K ras mutations 48 alpha synuclein 48 precocious puberty 48 heterozygotes 48 GIST tumors 48 bowel cancers 48 chitinase 48 KIF6 gene 48 cybrids 48 germ cells 48 epigenetic 48 GSTP1 48 genetically engineered mice 48 inherited retinal degeneration 48 tumor suppressor protein 48 neurofibrillary 48 KRAS oncogene 48 syngeneic 48 Wilm tumor 48 SIRT3 48 IL#R 48 ependymoma 48 HER2 gene 48 apoC III 48 hereditary spastic paraplegia 48 Sjögren syndrome 48 chromosome rearrangements 48 KCNQ1 48 PHLPP 48 proband 48 Epstein Barr virus 48 p# mutation 48 underactive thyroid gland 48 anencephaly 48 SGK1 48 MnSOD 48 motor neuron diseases 48 OGG1 48 HPV# 48 bacterium 48 peptide antigens 48 motor neuron degeneration 48 tumor suppressor genes 48 FTO variant 48 Retinoblastoma 48 infective agent 48 HLA alleles 48 immunodeficient 48 G#D 48 NKX2 48 Rad# 48 transthyretin 48 genetically susceptible 48 congenital anomaly 48 heritable 48 Newborn screening 48 polycystic kidneys 48 ectodermal dysplasia 48 pernicious anemia 48 GABAergic neurons 48 BARD1 48 Cowden syndrome 48 chromosomal translocations 48 autistic regression 48 signaling molecule 48 tau proteins 48 tau gene 48 mycobacterium tuberculosis 48 autosomal 48 TSP1 48 mRNA transcripts 48 adrenal function 48 IDH mutations 48 thymus gland 48 Hutchinson Gilford Progeria Syndrome 48 homozygosity 48 iPS cells 48 transgene 48 Th# cells 48 LRP5 48 DEC2 48 NKT cells 48 Salmonella typhi 48 BRAF protein 48 medulloblastomas 48 disease vCJD 48 MAOA gene 48 luminal cells 48 Meckel Gruber syndrome 48 neural cells 48 alpha thalassemia 48 CYP#C# * 48 Dpp 48 cystic fibrosis CF 48 epigenetic alterations 48 skeletal muscle actin 48 hereditary blindness 48 glucocerebrosidase 48 PrPSc 48 Pten 48 HLA identical 48 CYP#E# gene 48 SOD1 protein 48 tumor suppressor p# 48 G6PD 48 Plasmodium parasites 48 chromosomal translocation 48 bone marrow stem cells 48 chromosome #q# [001] 48 amyloid proteins 48 MSH6 48 roseola 48 CCR5 gene 48 abnormal proteins 48 sortilin 48 MYH9 48 ACE2 gene 48 mastocytosis 48 prion infection 48 Joubert syndromes 48 undergo apoptosis 48 ferroportin 48 truncus arteriosus 48 inherited gene mutation 48 Fas ligand 48 connexin 48 enzyme 48 germline stem cells 48 desmin 48 Smith Lemli Opitz syndrome 48 autosomal dominant polycystic kidney 48 G allele 48 VUR 48 deleterious mutation 48 CYP#D# gene 48 T. gondii 48 genes BRCA 48 epigenetic markers 48 NPHP 48 excess mucous 48 retinoic acid 48 Cystic fibrosis CF 48 primary pulmonary hypertension 48 acute myelogenous leukemia AML 48 prion protein PrP 48 NKX#.# 48 receptor gene 48 FASPS 48 lysosomal storage diseases 48 lymphocytic choriomeningitis virus LCMV 48 donor marrow 48 eosinophilic esophagitis 48 misfolded 48 TMEM#B 48 FOXP2 gene 48 HLHS 48 secretes insulin 48 abnormal methylation 48 TSC1 48 GRK2 47 IDH2 47 tau protein 47 Progeria 47 MHC molecules 47 BRCA1 gene mutation 47 Fragile X. 47 MEF2A 47 mesotheliomas 47 APOE ε4 47 ADAM# 47 neurologic disorder 47 Notch1 47 Cx# [001] 47 brain lesions 47 trypanosome 47 PTLD 47 familial dysautonomia 47 protein misfolding 47 IRS1 47 Pax6 47 ABCB1 47 CHD5 47 congenital cataract 47 ADAMTS# 47 transplanted stem cells 47 interferon pathway 47 rare chromosomal disorder 47 insulin resistance 47 aneuploidies 47 microsatellite instability 47 p# protein 47 TGFBR1 47 systemic amyloidosis 47 dilated cardiomyopathy 47 immunodeficiency 47 fructose intolerance 47 CGG repeats 47 nonischemic 47 PCNSL 47 amniotic fluid embolism 47 bacterial vaginosis 47 Lrp5 47 pleural mesothelioma 47 autoimmune disease 47 LPA gene 47 SLC#A# [002] 47 leptin receptor 47 underactive thyroid 47 Y chromosomes 47 fertilized egg splits 47 progranulin mutations 47 meningococcus 47 CFH gene 47 monozygotic twin 47 ARID1A 47 DISC1 gene 47 Tay Sachs thalassemia 47 systemic scleroderma 47 ADDLs 47 gene BRCA2 47 Karayiorgou 47 ovarian hormones 47 Niemann Pick type 47 bowel polyps 47 NAFLD 47 hair follicle stem cells 47 retinal dystrophy 47 CFTR 47 JAK2 gene 47 gene rearrangements 47 chromosomal anomalies 47 C. pneumoniae 47 prion proteins 47 genomic instability 47 genomic imprinting 47 recessive dystrophic epidermolysis bullosa 47 bronchopulmonary dysplasia 47 Prion proteins 47 cyclin D1 47 retinoblastoma Rb 47 Rb gene 47 V Leiden 47 gut microbes 47 tumor specific antigen 47 angiosarcoma 47 HLA B 47 intractable epilepsy 47 chromosome #q 47 Hsp# [001] 47 mitochondrial DNA 47 thyroid deficiency 47 immune suppression 47 diabetes insipidus 47 poorer prognosis 47 defensin 47 mutant huntingtin protein 47 clusterin 47 retinal dysfunction 47 Celiac disease 47 mitochondria 47 polycystic ovaries 47 Leber hereditary optic neuropathy 47 Notch signaling 47 mouse embryos 47 intestinal polyps 47 AAT Deficiency 47 Marfan 47 murine leukemia virus 47 molecular abnormalities 47 embryonal rhabdomyosarcoma 47 homologs 47 retinal cells 47 Alu elements 47 lentiviruses 47 ARVC 47 recessive 47 JAK2 enzyme 47 acute promyelocytic leukemia 47 symptomless 47 motor neuron disease 47 NNRTI resistance 47 preeclampsia 47 immature dendritic cells 47 SIRT1 gene 47 Hepatitis B virus 47 SIRT6 47 Usher Syndrome 47 sickle cell disease 47 ETV1 47 Prader Willi syndrome 47 amyloid protein 47 PKM2 47 Hypophosphatasia 47 chromosomal defects 47 histone modification 47 diaphragmatic hernia 47 CagA 47 genetic makeup 47 leptin 47 congenital abnormality 47 RCAN1 47 NFKBIA 47 alternatively spliced 47 pancreas 47 recurrent infections 47 H#Y mutation 47 primary biliary cirrhosis 47 tumors 47 MDM2 47 BRCA1 BRCA2 47 FADS2 47 Polycystic kidney disease 47 von Hippel Lindau 47 prosopagnosia 47 primary ovarian insufficiency 47 breast carcinomas 47 virulence genes 47 Th2 cells 47 HMGCR 47 endocrine disorder 47 proto oncogene 47 familial hypercholesterolemia FH 47 olfactory receptor 47 protein 47 Pin1 47 piRNAs 47 frameshift mutation 47 varicocele 47 pulmonary stenosis 47 adrenal cortex 47 haptoglobin 47 LRRK2 mutations 47 variable immunodeficiency 47 NR#A# gene 47 PTEN mutations 47 pluripotent cells 47 inflammatory bowel disease 47 abnormal Pap 47 mutant huntingtin 47 shorter telomeres 47 multidrug resistance 47 corneal cells 47 genes encoding 47 spastic diplegia 47 infection progressive multifocal 47 suppressor gene 47 chromosomes 47 arrhythmogenic right 47 pilocytic astrocytomas 47 glutamic acid decarboxylase 47 miRNAs 47 viral proteins 47 lamin 47 acute lymphoid leukemia 47 haplotypes 47 PTEN protein 47 congenital blindness 47 osteogenesis imperfecta 47 juvenile myelomonocytic leukemia 47 thyroiditis 47 SRY gene 47 GPC5 47 variant allele 47 CDKN2A 47 chaperone proteins 47 clotting disorder 47 PARP inhibition 47 hypermethylated