heterozygosity

1000	mutations
418	genotype
406	genes
406	gene
403	phenotype
402	alleles
401	mutation
397	allele
396	phenotypic
391	loss

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More distant neighbors

degeneration atrophy anemia susceptibility gastrointestinal abnormal cancers neuropathy deficiency tumors thyroid dopaminergic neuronal toxicity vitro abnormalities serotonin genetic hemoglobin epigenetic inflammation specificity estrogen urinary genotypes impairment tumor organism androgen heterogeneity oxidative inhibition neurological irreversible gastric chromosomal lesions testosterone dysfunction

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