autosomal dominant

Related by string. Autosomal dominant * : autosomal dominant polycystic kidney . autosomal recessive . autosomal recessive disorder . autosomal recessive disease . autosomal recessive genetic / Dominant . DOMINANT . dominants : dominant Fatah faction . dominant Kikuyu tribe . dominant Hawiye clan . Mogadishu dominant Hawiye * autosomal dominant disorder . autosomal dominant inheritance *

Related by context. Frequent words. (Click for all words.) 67 idiopathic 67 NF1 67 fatal neurodegenerative 66 neurodegenerative disorder 65 progressive degeneration 64 heterozygous 63 genetically inherited 63 phenotype 63 myotonic dystrophy 62 homozygous 62 genetic abnormality 62 von Willebrand disease 62 neoplasm 62 demyelination 62 frontotemporal dementia 62 familial hypercholesterolemia 62 hereditary disorder 61 nonsense mutation 61 chromosomal abnormality 61 parkinsonism 61 systemic lupus erythematosus SLE 61 Insulin resistance 61 immunodeficiency 60 genetic defect 60 beta thalassemia 60 nonsense mutations 60 mutated gene 60 T2DM 60 mutation 60 Cushing syndrome 60 degenerative disorder 60 myeloid 59 Retinopathy 59 neurological dysfunction 59 susceptibility gene 59 downregulation 59 VUR 59 hyperplasia 59 systemic lupus erythematosus 59 FSGS 59 Fragile X Syndrome 59 LQTS 59 Congenital 59 defective gene 59 heritable 59 enzyme deficiency 59 atopic 58 subtype 58 neuroendocrine 58 alleles 58 mutant gene 58 Fanconi anemia 58 phenylketonuria 58 Obstructive sleep apnea 58 progressive degenerative 58 osteogenesis imperfecta 58 recessive gene 58 cerebellar 58 relapsing remitting 57 retinal degeneration 57 metabolic abnormalities 57 myelodysplastic syndrome MDS 57 neoplastic 57 Overexpression 57 Spina bifida 57 Diabetic retinopathy 57 dystrophy 57 neuropsychiatric disorders 57 Gestational diabetes 57 haplotype 57 Friedreich ataxia 57 receptor gene 57 Fibrosis 57 aneuploidy 57 Cystic fibrosis 57 mutations 57 hypercalcemia 57 acute myelogenous leukemia AML 56 genetic mutation 56 atopy 56 primary biliary cirrhosis 56 long QT syndrome 56 subclinical 56 APOE4 56 acquired immunodeficiency syndrome 56 CYP#C# [002] 56 gene mutation 56 adenocarcinomas 56 mitochondrial dysfunction 56 dysregulated 56 T2D 56 genetic disorder 56 histologically 56 Osteosarcoma 56 ataxia 56 poorer prognosis 56 trisomy 56 non alcoholic steatohepatitis 56 congenital anomalies 56 mRNA expression 56 CNVs

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