autosomal recessive disease, embryonal rhabdomyosarcoma, myotonic muscular dystrophy, myotonic dystrophy, chromosomal anomaly, lymphocytic leukemia, monozygotic twin, generalized epilepsy, alveolar rhabdomyosarcoma, osteopetrosis, achromatopsia, degenerative disorder, retinitis, dermatomyositis, lymphoblastic leukemia, myoclonus, autosomal dominant disorder, myelomeningocele, erythematosus, erythema nodosum, neurosensory, plexiform, dysgenesis, lupus erythematosus, carcinoid, orchitis, neurofibromas, myositis, hyperinsulinism, rheumatic disease, monocytic, neurogenic bladder, xeroderma pigmentosum, heterotaxy, glomerulonephritis, monogenic, proband, syngeneic, arteritis, leukodystrophy, bullous, dystrophy, blastoma, leydig cell, histiocytosis, nonhereditary, duchenne, cholestasis, hamartoma, hypercalciuria, atopic eczema, wilms tumour, dysphasia, thyrotoxicosis, cryptogenic, achondroplasia, arthropathy, muscular dystrophy, osteogenesis imperfecta, lichen planus, lymphocytic, valvular heart disease, nephritis, idiopathic thrombocytopenic purpura, idiopathic, myotonia, hemiplegia, severe combined immunodeficiency, herpes encephalitis, nephrotic syndrome, thyroiditis, epithelioid, fibroma, astrocytoma, hypercalcaemia, essential tremor, rhabdoid, aplasia, molar pregnancy, herpes zoster virus, urethritis, hemolytic anemia, myelopathy, superior mesenteric artery, pyloric stenosis, syringomyelia, nephrosis, mody, familial hypercholesterolemia, hypopituitarism, rhabdomyosarcoma, galactosemia, proteoglycan, hyperalgesia, lacunar, myasthenia gravis, dyskinetic, epididymitis, roseola, neuromotor, meningoencephalitis, hemophilia b