homozygous

1000	heterozygous
709	allele
657	recessive
652	phenotype
644	gene
629	mutations
625	genes
611	mutation
608	alleles
604	deficiency

previous:	homozygotes
next:	HOMR
random:	Tilhance

More distant neighbors

abnormal abnormalities autosomal chromosome genotype chromosomal tissues symptoms chromosomes infection syndrome antibodies anemia tumors genetic tissue lesions adrenal gastrointestinal congenital hormone abnormality metabolic fetal tumor inflammation immune intestinal marrow liver thyroid organism trait asymptomatic bacterial necrosis insulin DNA infections

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