Related by context. All words. (Click for frequent words.) 75 recessive genes 71 mutated gene 70 recessive trait 69 defective gene 67 mutant gene 64 genetic mutation 63 genetic trait 63 gene mutation 62 genetic defect 62 autosomal recessive disease 62 mutation 61 autosomal recessive 61 abnormal hemoglobin 61 heterozygous 61 genetic abnormality 59 chromosomal abnormality 59 alleles 58 aY chromosome 58 autosomal dominant 58 Tay Sachs disease 57 MC1R gene 57 maternally inherited 57 recessive 57 X chromosome 57 recessive genetic 57 chromosome abnormality 57 spontaneous mutation 57 genetic variant 57 G#S mutation 57 holoprosencephaly 56 homozygous 56 Apert syndrome 56 genes predisposing 56 recessive traits 55 chromosomal defect 55 chromosomal disorder 55 CFTR gene 55 inherited mutations 55 polydactylism 55 APOE gene 55 BRCA1 gene 55 missense mutation 55 ApoE4 gene 55 Fragile X gene 55 de novo mutations 55 mutant allele 55 X chromosomes 54 genetic defects 54 APOE4 54 MC1R 54 mosaicism 54 Rh positive 54 Beckwith Wiedemann syndrome 54 TP# mutation 54 mutations 54 recessive mutations 54 allele 54 autosomal recessive disorder 53 BRCA2 gene 53 genetically inherited 53 myostatin gene 53 albinism 53 MYH9 gene 53 recessive mutation 53 Fanconi anemia 53 congenital disorder 53 Fraternal twins 53 beta thalassemia 53 genetically identical 53 gene variant 53 ApoE gene 53 GFP gene 53 sickle hemoglobin 53 Li Fraumeni syndrome 53 Spinal muscular atrophy 53 inbreeding depression 52 hereditary deafness 52 MECP2 gene 52 homozygosity 52 RPE# 52 genetic disorder 52 recessive genetic disorders 52 toxoplasmosis 52 Angelman syndrome 52 CNTNAP2 gene 52 C#Y 52 fetal hemoglobin 52 heritable 52 Dravet syndrome 52 mtDNA mutations 52 HLA genes 52 mutated genes 52 ApoE4 52 Cockayne syndrome 52 SRY gene 52 gene mutations 52 pyloric stenosis 52 disease epidermolysis bullosa 52 chromosomal anomaly 52 offspring 52 BARD1 52 abnormal chromosome 52 LRRK2 gene 51 hypertrichosis 51 neural tube defect 51 genetic mutations 51 Spina bifida 51 incomplete penetrance 51 mutant genes 51 chromosome deletion 51 genetic abnormalities 51 VHL gene 51 IGF2 51 germline mutations 51 proband 51 Kufs disease 51 congenital disorders 51 APOE4 gene 51 genomic imprinting 51 rhesus 51 CCR5 delta# 51 fatal neurodegenerative 51 RDEB 51 BRCA1 mutation 51 pigment melanin 51 spontaneous mutations 51 FMR1 gene 51 xeroderma pigmentosum 51 genetically 51 gene 51 Tay Sachs 51 dizygotic twins 51 microfilariae 51 galactosemia 51 fertilized egg splits 51 nonhereditary 50 HFE gene 50 HLA B# 50 herpes infection 50 enzyme deficiency 50 NF1 50 Leptospira 50 Male pattern baldness 50 germline cells 50 MLL gene 50 DiGeorge syndrome 50 Meckel Gruber 50 hereditary disorder 50 susceptibility gene 50 single celled parasite 50 STAT4 50 incurable genetic 50 monozygotic twins 50 BRIP1 50 melanistic 50 apolipoprotein E gene 50 asymptomatically 50 overo 50 gene variation 50 imprinted genes 50 Klinefelter syndrome 50 LIS1 50 dysgenesis 50 IgA deficiency 50 pneumococci 50 primordial germ cells 50 thalassemia trait 50 inherited predisposition 50 herpes viruses 50 Joubert syndrome 50 achromatopsia 50 lightly pigmented 50 hypertrophic cardiomyopathy HCM 50 sexually dimorphic 50 Crouzon syndrome 49 congenital adrenal hyperplasia CAH 49 BRCA2 mutation 49 autosomal dominant disorder 49 congenital abnormality 49 polydactyly 49 OCA2 49 IGF1 49 genetic predisposition 49 SMN1 gene 49 LPA gene 49 breast cancer genes BRCA1 49 dominantly inherited 49 familial ALS 49 prion gene 49 BRCA2 breast cancer 49 Toxoplasmosis 49 parthenogenetic 49 rare chromosomal disorder 49 prion protein gene 49 dizygotic 49 selfing 49 neuroblastomas 49 MTHFR 49 CHD7 49 Niemann Pick disease 49 hyperemesis gravidarum 49 precocial 49 V Leiden 49 Fragile X syndrome 49 alpha thalassemia 49 Fragile X Syndrome 49 WAGR syndrome 49 TCF#L# gene 49 D. melanogaster 49 Lafora disease 49 progranulin gene 49 familial adenomatous polyposis 49 congenital deafness 49 Coronaviruses 49 Hashimoto thyroiditis 49 microcephalin 49 nongenetic 49 monozygotic twin 49 mutant alleles 49 Babesia 49 globin 49 TGFBR1 * 6A 49 RPE# gene 48 breast cancer gene mutation 48 #q#.# deletion syndrome 48 trypanosome 48 mice lacking 48 lissencephaly 48 Diamond Blackfan anemia 48 chromosomal disorders 48 R. equi 48 Plasmodium parasites 48 tapeworm infection 48 fibrodysplasia ossificans progressiva FOP 48 APOE ε4 48 herpes virus 48 monozygotic 48 HLA identical 48 heritable genetic 48 filaggrin 48 aniridia 48 haploid 48 APOE epsilon 4 48 APOE 48 TACI mutations 48 trisomy 48 septo optic dysplasia 48 granulosa cell 48 phenotypic variation 48 LRAT 48 huntingtin gene 48 UGT#B# 48 genetic 48 Genetic mutations 48 MCAD deficiency 48 phthalate syndrome 48 recessive inheritance 48 chromosomal alterations 48 congenital anomaly 48 maternal antibodies 48 chromosome rearrangements 48 autosomal 48 abnormal prions 48 Retinoblastoma 48 anencephaly 48 ichthyosis 48 premutation 48 severe congenital neutropenia 48 microdeletion 48 mutated BRCA1 48 HLA DQ2 48 asymptomatic carriers 48 SHANK3 48 Becker muscular dystrophy 48 neuroligins 48 APOE e4 48 autosomal recessive genetic 48 nonsense mutations 48 Bardet Biedl syndrome 48 aneuploidy 48 developmental abnormalities 48 FASPS 48 reassortants 48 FXTAS 48 mitochondrial mutations 48 agouti gene 48 pea aphid 48 genetic alteration 48 apoE4 48 neurodevelopment disorder 48 mammary tumors 48 HLA B# gene 48 neurodevelopmental disorder 48 haplogroups 48 Wiskott Aldrich syndrome 48 diploid 48 Alport syndrome 48 hereditary hemochromatosis 47 HNPCC 47 ambiguous genitalia 47 epigenetic changes 47 maternally transmitted 47 cryptorchidism 47 mangabeys 47 BRCA mutation 47 SLC#A# [001] 47 recessively inherited 47 Dwarfism 47 olfactory receptor 47 COMT gene 47 leucistic 47 varicella zoster virus 47 gene APOE4 47 Ehrlichia 47 immunodeficiency 47 abnormal chromosomes 47 DiGeorge Syndrome 47 OCA2 gene 47 CCR5 mutation 47 pseudotumor cerebri 47 osteogenesis imperfecta 47 roseola 47 Wwox 47 Hutchinson Gilford progeria 47 klotho 47 genes 47 biological predisposition 47 Toxoplasma 47 neural crest cells 47 Vitamin B# deficiency 47 serotonin defects 47 FOXP2 gene 47 Leber congenital amaurosis 47 MSH2 47 G allele 47 phenotypically 47 prion infection 47 neurodegenerative disorder 47 ApoE4 allele 47 Neuregulin 1 47 genetic variation 47 inherited genetic mutation 47 CNVs 47 hemochromatosis 47 Hirschsprung disease 47 Sickle cell 47 heterozygotes 47 immunodeficiency disorder 47 inherited neurological disorder 47 haplotype 47 lactase deficiency 47 achondroplasia 47 highly heritable 47 Anencephaly 47 herpesviruses 47 PTPN# 47 autistic regression 47 Hurler syndrome 47 FTO gene 47 UGT#A# * 47 Trypanosoma brucei 47 genetically predetermined 47 endocrine disorder 47 Usher Syndrome 47 APOE allele 47 merle 47 genetic traits 47 Rh factor 47 ectoderm 47 epigenetically 47 CETP VV 47 R#W [002] 47 polymorphism 47 hypoplasia 47 BRCA gene mutation 47 dermatophytes 47 DiGeorge syndrome rare 47 HYPP 47 HGPS 47 KIF6 gene 47 retinitis 47 trichromatic vision 47 BRCA1 gene mutation 47 fatal neuromuscular disorder 47 gametophyte 47 familial dysautonomia 47 OPRM1 gene 47 brucei 47 receptor gene 47 Wolbachia strains 47 alternatively spliced 47 mtDNA 47 histiocytosis 47 reproductively successful 47 orthologs 47 dyskeratosis congenita 47 wholphin 47 basal cell nevus syndrome 47 CDH1 47 colugos 47 familial pancreatic cancer 46 neurofibromas 46 Dental fluorosis 46 Heterozygous 46 protozoan parasite 46 monogenic 46 cowpox virus 46 epidermolysis bullosa EB 46 germline mutation 46 CFH gene 46 vesicular stomatitis virus 46 MAOA gene 46 TEL AML1 46 hemolytic disease 46 endogenous retroviruses 46 parasite Plasmodium falciparum 46 Lesch Nyhan syndrome 46 atopy 46 consanguineous marriage 46 reproduce asexually 46 multisystem disorder 46 ovules 46 limb malformations 46 epidermolysis bullosa 46 BRCA1 mutations 46 chronic granulomatous disease 46 brain malformation 46 spinal muscle atrophy 46 SMN2 gene 46 chromosomal abnormalities 46 sexually reproducing 46 ataxias 46 nonsense mutation 46 phenotype 46 genetically susceptible 46 VUR 46 congenital hypothyroidism 46 frameshift mutation 46 Rickettsia 46 Hemophilia B 46 undiagnosed celiac disease 46 Borrelia 46 #q# deletion 46 Severe Combined Immunodeficiency 46 chromosomal aberrations 46 reproductively isolated 46 MC4R gene 46 prion protein PrP 46 apolipoprotein E 46 G6PD deficiency 46 retinal dysfunction 46 infertility miscarriages 46 CYP#C# * 46 PB1 F2 46 BRCA gene 46 missense mutations 46 TP# gene 46 genes BRCA1 46 IL#R 46 chromosomal anomalies 46 microcephaly 46 cystic fibrosis Duchenne muscular 46 unspayed female cat 46 Genital herpes 46 Epstein Barr virus EBV 46 APOL1 46 autosomal dominant inheritance 46 parasiticus 46 genetic susceptibility 46 PrPSc 46 nonidentical 46 allelic variation 46 SLC#A# gene [001] 46 imperfecta 46 HLA DRB1 46 HMGA2 46 HLA molecules 46 heritable trait 46 filaggrin gene 46 KCNQ1 46 BRCA2 46 MCADD 46 ADPKD 46 myotonic dystrophy 46 degenerative disorder 46 CNTNAP2 46 toxoplasma gondii 46 CAG repeats 46 mitochondrial disease 46 mitochondrial DNA mutations 46 chromosome abnormalities 46 lipin 46 hereditary diseases 46 NF1 gene 46 genital abnormalities 46 Mycoplasma pneumoniae 46 parrots parakeets 46 squirrel pox virus 46 pox virus 46 RCAN1 46 canis 46 sCJD 46 MTHFR gene 46 MeCP2 gene 46 corona virus 46 Borrelia burgdorferi 46 penetrance 46 S. neurona 46 malignant transformation 46 polyploidy 46 GSTM1 gene 46 undescended testicles 46 FMR1 46 Nf1 46 chimeric mice 46 flavivirus 46 Mendelian 46 Congenital Adrenal Hyperplasia 46 DRD4 46 juvenile myelomonocytic leukemia 46 Retinitis pigmentosa 46 neurona 46 piRNAs 46 Genetic abnormalities 46 Polycystic kidney disease 45 Alu elements 45 mitochondrial defects 45 primordia 45 Zinc deficiency 45 naped 45 syringomyelia 45 chromosomal translocations 45 protein encoded 45 SMN1 45 combined immunodeficiency SCID 45 PDGFRA 45 placental function 45 recessive disorders 45 CCR5 gene 45 polyploid 45 habitual snoring 45 LQTS 45 C EBP alpha 45 IRAK1 45 fatal neurodegenerative disorder 45 Newborn screening 45 Epidermolysis bullosa 45 Foxp3 45 C. neoformans 45 heterozygote 45 spastic diplegia 45 K ras gene 45 male prairie voles 45 homozygotes 45 Menkes disease 45 sirenomelia 45 bacterium E. coli 45 parasite Trypanosoma cruzi 45 littermate 45 mutant protein 45 Joubert Syndrome 45 hydrops 45 Mitochondrial DNA 45 MHC genes 45 recessive dystrophic epidermolysis bullosa 45 synuclein 45 persistent pulmonary hypertension 45 parainfluenza virus 45 chromosomal defects 45 lactase gene 45 variable immunodeficiency 45 Wolf Hirschhorn 45 ChR2 45 APOC3 45 teratoma 45 #p#.# [001] 45 cybrids 45 meadow vole 45 Krabbe Leukodystrophy 45 heterozygosity 45 HMGA2 gene 45 endogenous retrovirus 45 Igf2 45 genetic variability 45 inbreeding 45 Heredity 45 Hypoplastic Left Heart 45 autosomes 45 mRNA transcripts 45 medium chain acyl 45 TP# mutations 45 genetic disorders 45 precocious puberty 45 p# mutation 45 ApoE 45 TOMM# 45 deleterious mutations 45 anaplasmosis 45 melanocyte stem cells 45 deleterious mutation 45 lactose tolerance 45 Genetic variation 45 sporadic Creutzfeldt Jakob 45 transcriptional repression 45 haplogroup 45 epigenetic modifications 45 parkin gene 45 Down syndrome chromosomal disorder 45 haplotypes 45 progerin 45 germline 45 DRD2 gene 45 apoC III 45 Mendelian disorders 45 Candida species 45 SCA5 45 exfoliation glaucoma 45 NF2 45 gene variants 45 prion disease 45 T. gondii 45 spontaneous remission 45 segmental duplications 45 polyploids 45 prosopagnosia 45 immunodeficient 45 Brugada Syndrome 45 Cryptococcus neoformans 45 beta globin 45 tetraploid 45 gene p# 45 BRCA2 gene mutation 45 genetically distinct 45 Y chromosomal 45 Wolbachia 45 Lactose intolerance 45 blastomeres 45 microchimerism 45 ultra rapid metabolizer 45 Rb gene 45 clade C 45 MLL2 45 experimentally infected 45 Helicobacter 45 Aplastic anemia 45 autoinflammatory 45 melanosomes 45 H5 viruses 45 Neanderthal genes 45 brain lesions 45 HbF 45 epigenetic inheritance 45 SOD1 protein 45 congenital CMV 45 poorer prognosis 45 MODY 45 placental mammals 45 SMN protein 45 asexual reproduction 45 Triticum 45 embryo biopsy 45 Osteosarcoma 45 laforin 45 toxoplasma 45 cerebri 45 Hutchinson Gilford Progeria Syndrome 45 socially monogamous 45 recurrent miscarriages 45 prolific breeders 45 allelic variants 45 chromosomal rearrangement 45 Rh incompatibility 45 gene rearrangements 45 SERT gene 45 endostatin 45 BRAC2 45 Smith Lemli Opitz syndrome 45 chromosomal deletions 45 polycystic ovary syndrome 45 human leukocyte antigen 45 ligers 45 susceptibility genes 45 TRIM5 44 ε4 44 sporadic ALS 44 mitochondrial dysfunction 44 auditory neuropathy 44 Hsp# [001] 44 ovulated 44 GPR# [002] 44 pneumococcal meningitis 44 TSC1 44 dyscalculia 44 ADAMTS# 44 Cystic fibrosis CF 44 congenital cataract 44 prion strains 44 Folic acid deficiency 44 Hip dysplasia 44 pelage 44 hereditary blindness 44 metabolic disorder 44 CIB1 44 inherited gene mutation 44 haemolytic anemia 44 modifier genes 44 Leydig cells 44 toxemia 44 Genetic mutation 44 CDKN2A 44 SHANK3 gene 44 JAK2 mutation 44 shorter telomeres 44 IKZF1 44 causative gene 44 ZNF# 44 nonidentical twins 44 dopamine receptor gene 44 antigenic shift 44 V#F mutation 44 genetic lineages 44 Crouzon Syndrome 44 PALB2 44 mitochondrial diseases 44 neurofibroma 44 primary ciliary dyskinesia 44 skeletal dysplasia 44 squirrel pox 44 genetic imprinting 44 BRCA mutations 44 acute lymphoid leukemia 44 transcriptional repressor 44 regulator CFTR gene 44 Kabuki syndrome 44 enterocolitis 44 outbred 44 Xenopus 44 G#S [002] 44 amniotic fluid embolism 44 ectodermal dysplasia 44 uterus didelphys 44 outcrossing 44 aneuploidies 44 Familial Dysautonomia 44 polydactyl 44 spinocerebellar ataxia 44 heterosis 44 dopamine transporter gene 44 M. leprae 44 hereditary disorders 44 coloration 44 murine leukemia virus 44 inbred strains 44 BRCA1 44 CHARGE syndrome 44 reassorted 44 IDH2 44 predisposing factor 44 retinitis pigmentosa RP 44 prairie vole 44 Penile cancer 44 lysosomal storage diseases 44 Hepatitis B virus 44 Usher syndrome 44 CYP#B# 44 mammary gland tumors 44 medulloblastoma tumors 44 agouti 44 Hutchinson Gilford Progeria 44 lineages 44 AAT deficiency 44 Selenium deficiency 44 legged ticks 44 homocystinuria 44 mutated K ras 44 heterotaxy 44 anti microbial peptides 44 Viral conjunctivitis 44 APOE e4 gene 44 Diptera 44 consanguineous 44 #q# [001] 44 conspecifics 44 PTEN mutation 44 FGFR2 44 NR#A# gene 44 genetic polymorphism 44 Tay Sachs Disease 44 von Willebrand disease 44 epigenetic silencing 44 lactase persistence 44 IUGR 44 retrovirus 44 multigenic 44 serotype 44 heritable traits 44 tumor suppressor gene 44 giant danio 44 BRAF gene 44 eosinophilic 44 Biliary atresia 44 diaphragmatic hernia 44 Asberger syndrome 44 homozygote 44 B. subtilis 44 SMN2 44 LRRK2 mutations 44 aldehyde dehydrogenase 44 familial hypercholesterolemia 44 siskin 44 Juravenator 44 Mycobacterium bovis 44 pubic lice 44 Joubert syndromes 44 Alleles 44 Von Hippel Lindau 44 mouse testes 44 AAV2 44 transfusion syndrome 44 X inactivation 44 retinoblastoma 44 p# mutations 44 NPC1 44 morphologically 44 Y chromosome 44 syngeneic 44 malformations 44 infective agent 44 genetically predisposed 44 Atopic dermatitis 44 clonal reproduction 44 CYP#D# gene 44 congenital cataracts 44 reassortant 44 Peromyscus 44 FADS2 44 chromosomal rearrangements 44 excitatory synapses 44 inhibitory receptor 44 Coeliac disease 44 gambiae 44 nematode worm 44 biliary atresia 44 subtype 44 mitochondrial disorders 44 side blotched lizards 44 vegetatively 44 simian immunodeficiency virus 44 Tay Sachs thalassemia 44 D. simulans 44 Pax6 44 sepals 44 rotaviruses 44 faulty BRCA1 gene 44 Sandhoff disease 44 Medulloblastoma 43 outgrow peanut allergy 43 MEF2A 43 ADA SCID 43 gene deletions 43 papillomaviruses 43 c KIT 43 JAK2 gene 43 clade B 43 histocompatibility 43 Mitochondrial Eve 43 hypogonadotropic hypogonadism 43 Plasmodium vivax 43 lichen planus 43 simian virus 43 YKL 43 bronchopulmonary dysplasia 43 mammary cells 43 trypanosomes 43 microsporidia 43 KLF# 43 mutated BRCA 43 Sporadic CJD 43 X chromosome inactivation 43 evolutionary lineage 43 Mendelian diseases 43 immunodeficiencies 43 classical scrapie 43 paraneoplastic 43 Niemann Pick 43 Genetic predisposition 43 LMNA gene 43 #q#.# [001] 43 Beta thalassemia 43 PTCHD1 gene 43 dwarfism 43 microdeletions 43 Noonan Syndrome 43 epigenetic alterations 43 adrenal cortex 43 subclinical 43 gene MECP2 43 phenotypic expression 43 naturally occurring fungus 43 endosymbiosis 43 undescended testicle 43 clade 43 von Hippel Lindau 43 dedifferentiation 43 fatty liver disease 43 fungus infects 43 KIBRA 43 transmissible spongiform encephalopathies 43 aneuploid 43 XX chromosomes 43 activating mutations 43 genetic makeups 43 Prox1 43 congenital abnormalities 43 SOD2 gene 43 androgen receptor gene 43 Colorectal cancers 43 genetic syndromes 43 Peutz Jeghers syndrome 43 GRK5 43 A. thaliana 43 causative mutation 43 unspecialized 43 rhodopsin 43 premature ovarian 43 polygenic 43 T. vaginalis 43 suppressor gene 43 distantly related species 43 aciduria 43 genomic instability 43 Sanfilippo syndrome 43 Leber Congenital Amaurosis 43 pre eclamptic 43 twin transfusion 43 anopheles 43 hemophagocytic lymphohistiocytosis 43 Treg cell 43 SORL1 43 JAK mutations 43 malformation 43 parasitic worm 43 osteopetrosis 43 ENPP1 43 aneuploid cells 43 chimeric 43 sifaka 43 mucins 43 SGK1 43 K#R [002] 43 EBV infection 43 hoofed mammals 43 GISTs 43 causative genes 43 clonally 43 MnSOD 43 P. falciparum 43 Burkholderia 43 variant alleles 43 evolutionary lineages 43 mental retardation epilepsy 43 retinal degeneration 43 HLA gene variant 43 congenital blindness 43 SOX3 gene 43 Ets2 43 genetic makeup 43 cystic hygroma 43 haemochromatosis 43 parasitoid wasp 43 HTLV 43 hermaphrodites 43 chromosomal instability 43 mycobacterium tuberculosis 43 truncus arteriosus 43 Ras oncogene 43 fronto temporal dementia 43 morphological traits 43 brood parasitism 43 castrated males 43 M. pneumoniae 43 chordate 43 Toxoplasma gondii 43 chromosomally abnormal 43 susceptibility alleles 43 LCMV virus 43 giant peccary 43 CYP#E# gene 43 germline stem cells 43 Cushing syndrome 43 Vitamin D insufficiency 43 mutant strain 43 trichomonosis 43 leptin deficiency 43 homozygous FH 43 Mariamene 43 TAp# 43 NPHP 43 inherited retinal degeneration