autosomal recessive disease, phenylketonuria, familial hypercholesterolemia, autosomal dominant disorder, becker muscular dystrophy, myotonic dystrophy, hemophilia b, acne vulgaris, galactosemia, anemias, mosaicism, generalized epilepsy, proband, osteogenesis imperfecta, syngeneic, carcinoid, pheochromocytoma, diabetes mellitus, iddm, myeloid, embryonal rhabdomyosarcoma, rhabdomyosarcoma, immunodeficiency, leydig cell, metabolic disorder, lupus erythematosus, glomerulonephritis, hyperinsulinism, severe combined immunodeficiency, hyperbilirubinemia, leukodystrophy, thyrotropin, xeroderma pigmentosum, heterotaxy, rheumatic disease, genetic abnormality, lymphoblasts, hemolytic anemia, chromosomal anomaly, b lymphocyte, rhd, neurofibromas, lactase deficiency, parainfluenza virus, genetic defect, factor xiii, myelomeningocele, purpura, systemic lupus erythematosus, triiodothyronine, leiomyoma, lichen planus, medulloblastoma, hypoparathyroidism, degenerative disorder, klinefelter syndrome, autoantibodies, hypopituitarism, erythematosus, subtype, ascus, lymphoblastic leukemia, haemolytic anemia, ichthyosis, pernicious anemia, genetic disorder, histiocytosis, pyloric stenosis, homozygosity, orchitis, dysgraphia, monozygotic twin, seminoma, teratoma, achondroplasia, hyperkalemia, atopic eczema, essential tremor, hypercalciuria, enteropathy, coprolalia, monoamine oxidase, steroidogenesis, pulvinar, isoenzymes, penetrance, eoe, gene mutation, hyperplasia, pyelonephritis, social phobia, urethritis, hyperparathyroidism, osteomalacia, choriocarcinoma, juvenile diabetes, myotonic muscular dystrophy, lymphocytic, hydrops, monocytic, cryptogenic, hydroxylase