neurofibromatosis, degenerative disorder, histiocytosis, blastoma, myotonic muscular dystrophy, cerebri, osteopetrosis, hydrocephaly, nephritis, embryonal rhabdomyosarcoma, osteogenesis imperfecta, autosomal dominant disorder, lymphocytic leukemia, alveolar rhabdomyosarcoma, choriocarcinoma, retinitis, fibroma, autosomal recessive disease, genetic disorder, dystrophy, ichthyosis, angiosarcoma, rhabdomyosarcoma, neurogenic bladder, becker muscular dystrophy, metabolic disorder, neurofibromas, polycystic kidney disease, achondroplasia, dysphasia, achromatopsia, carcinoid, aplastic anaemia, klinefelter syndrome, severe combined immunodeficiency, xeroderma pigmentosum, arthropathy, lymphoblastic leukemia, dysgenesis, aplasia, cutis, atresia, plexiform, syringomyelia, agenesis, nephrosis, muscular dystrophy, kawasaki disease, hydrops, generalized epilepsy, congenital disorder, wilms tumour, osteogenic sarcoma, myotonic dystrophy, teratoma, congenital anomaly, myelomeningocele, glomerulonephritis, bulbar, hemolytic anemia, demyelination, hemiplegia, purpura, idiopathic thrombocytopenic purpura, neurological disorder, lymphocytic, epilepsy, genetic abnormality, thyroiditis, rh incompatibility, malformation, diaphragmatic hernia, hypoplasia, anemias, essential tremor, neuroblastoma, congenital abnormality, epithelioid, hyperinsulinism, hemangioma, lichen planus, familial hypercholesterolemia, leiomyosarcoma, torticollis, polymyositis, monocytic, rhabdoid, myelitis, pheochromocytoma, hypotonia, leydig cell, cerebral palsy, astrocytoma, retinitis pigmentosa, neuritis, paresis, meningeal, galactosemia, myositis, myelopathy, paraplegia, ataxia, rickets, cardiomyopathy, immunodeficiency, myopathies, myopathy, epilepsies, idiopathic, dystrophies, hemochromatosis, parkinsonism, thrombocytopenia, amyloidosis, cerebellar, dystonia, encephalopathies, glaucoma, hypoparathyroidism