autosomal dominant disorder, becker muscular dystrophy, mosaicism, chromosomal anomaly, proband, nonhereditary, monogenic, genus plasmodium, hemophilia b, dysgenesis, lymphoblasts, phenothiazines, syngeneic, galactosemia, deoxy, rh positive, enkephalin, choriocarcinoma, glomerulonephritis, heterozygote, leydig cell, plexiform, monocytic, herpesviruses, lichen planus, lymphocytic, metaplasia, hydrops, orchitis, histiocytosis, severe combined immunodeficiency, monozygotic twin, erythematosus, heterozygous, amebiasis, epiglottitis, hydrolase, trophoblastic, chlamydial, immunopathology, generalized epilepsy, hepatoma, pheochromocytoma, synthetase, familial hypercholesterolemia, c. trachomatis, leucopenia, idiopathic thrombocytopenic purpura, factor xiii, recessive gene, mycobacterium tuberculosis, penetrance, vivax, cerebri, hypocalcaemia, encephalomyelitis, hyperparathyroidism, haematopoietic, cytopathic, glycopeptide, lactase deficiency, aplasia, corynebacterium, arteritis, osteopetrosis, roseola, xeroderma pigmentosum, epididymitis, superior mesenteric artery, peroxisome, meningococcus, cytotoxin, urethritis, myoclonus, bullous, mineralocorticoid, superoxide dismutase, nephrosis, rh incompatibility, anemias, autosomal, haemolytic anemia, nonvascular, pyloric stenosis, enterotoxin, achromatopsia, xenopus laevis, amnestic, isomerase, borrelia burgdorferi, isoenzymes, hydroxylase, treponema, etiologic, hypercalciuria, lacunar, hyperplastic, presymptomatic, orthopoxvirus, lymphoblastic leukemia, hypoplasia, thyrotropin

infantile amaurotic idiocy, niemann-pick disease, sachs disease, tay-sachs, tay-sachs disease, thrombasthenia

congenital disease, genetic abnormality, genetic disease, genetic disorder, inherited disease, inherited disorder