Related by context. Frequent words. (Click for all words.) 66 FAMILION 64 familial hypercholesterolemia 61 LQTS 61 genetic polymorphisms 60 AAT deficiency 60 breast cancer metastasis 60 Fragile X Syndrome 60 FTLD 59 congenital disorders 59 CYP#C# [002] 59 CFTR gene 59 HNPCC 59 anemias 58 susceptibility gene 58 Alzheimer Disease AD 58 sporadic ALS 58 muscular dystrophies 58 Fanconi anemia 57 molecular biomarkers 57 Alzheimers disease 57 hemolytic anemia 57 Duchenne muscular dystrophy DMD 57 Long QT Syndrome 57 acute promyelocytic leukemia 57 Leber congenital amaurosis 57 degenerative disorder 57 thrombophilia 57 chromosomal disorder 56 pleural mesothelioma 56 V Leiden 56 neurodegenerative disorder 56 NF1 56 Polycystic Kidney Disease 56 T2D 56 mutant genes 56 mutated genes 56 BRCA2 gene 55 Retinoblastoma 55 FMR1 gene 55 GeneChip 55 myotonic dystrophy 55 lung fibrosis 55 genetically inherited 55 APOE gene 55 malignant pleural mesothelioma 55 K RAS 55 Cystic Fibrosis CF 55 lung adenocarcinoma 55 genetic defect 55 genetic abnormality 55 Newborn screening 55 protein misfolding 55 pharmacogenetic 55 thyroid dysfunction 55 frontotemporal dementia 54 genetic defects 54 multidrug resistance 54 Cockayne Syndrome 54 CYP#C# [001] 54 hemochromatosis 54 Muscular dystrophy 54 genetic underpinnings 54 nonsense mutations 54 Retinopathy 54 colorectal cancer CRC 54 APOE4 54 MTHFR 54 Ambry Genetics 54 FLT3 54 ovarian breast 54 Gliomas 54 autosomal 54 galectin 3 54 myelodysplasia 54 carcinoid 54 genetic abnormalities 54 hereditary breast 54 ependymoma 54 CYP#D# 54 neurological illnesses 54 DiGeorge syndrome 54 disease NAFLD 54 susceptibility genes 54 myeloproliferative disorders 54 cardiac hypertrophy 54 nonsense mutation 53 myeloid leukemia 53 Parkinson disease PD 53 phenylketonuria 53 Friedreich ataxia 53 genetic determinants 53 ARVC 53 enzyme deficiency 53 genetic variations 53 Glioma 53 colorectal polyps 53 vitamin B# deficiency 53 Patient Registry 53 genetic mutations 53 aneuploidy 53 human leukocyte antigen