mutant gene, genetic mutation, gene mutation, genetic defect, autosomal recessive disease, genetic abnormality, heterozygous, alleles, homozygous, recessive, polydactylism, rh positive, mosaicism, albinism, genetic disorder, heritable, congenital disorder, homozygosity, offspring, toxoplasmosis, chromosomal anomaly, proband, pyloric stenosis, rhesus, hypertrichosis, genetically, galactosemia, gene, nonhereditary, dysgenesis, autosomal dominant disorder, xeroderma pigmentosum, polydactyly, hyperemesis gravidarum, melanistic, congenital abnormality, precocial, herpesvirus, dizygotic, parthenogenetic, nongenetic, monozygotic twin, achromatopsia, globin, anencephaly, trisomy, monozygotic, meningococcus, haploid, congenital anomaly, autosomal, herpes virus, ichthyosis, aneuploidy, diploid, rh factor, cryptorchidism, immunodeficiency, mangabeys, hypoplasia, osteogenesis imperfecta, merle, roseola, trypanosome, lactase deficiency, ectoderm, herpesviruses, ovules, achondroplasia, varicella zoster virus, gametophyte, retinitis, tapeworm infection, haplotype, polymorphism, becker muscular dystrophy, monogenic, atopy, hemochromatosis, vivax, hemophilia b, mendelian, coccidia, myotonic dystrophy, herpes zoster virus, genus plasmodium, phenotype, penetrance, canis, rh negative, polyploidy, histiocytosis, borrelia burgdorferi, microcephaly, inbreeding, lipin, neurofibromas, hydrops, severe combined immunodeficiency, teratoma, heterozygote