achondroplasia, genetic disorder, congenital disorder, diaphragmatic hernia, cerebral palsy, neurofibromatosis, rhabdomyosarcoma, congenital abnormality, atresia, idiopathic, polycystic kidney disease, degenerative disorder, metabolic disorder, torticollis, genetic abnormality, hydrops, thyroiditis, spina bifida, myotonic dystrophy, lactase deficiency, leukodystrophy, histiocytosis, embryonal rhabdomyosarcoma, malformation, myelomeningocele, pyloric stenosis, osteogenic sarcoma, juvenile rheumatoid arthritis, autosomal dominant disorder, scoliosis, dwarfism, aplastic anemia, genetic defect, hemangioma, dermatomyositis, hypotonia, lymphoblastic leukemia, apraxia, rheumatic disease, galactosemia, blastoma, chromosomal anomaly, agenesis, osteopetrosis, birth defect, lymphocytic leukemia, becker muscular dystrophy, syringomyelia, neurological disorder, fibroma, hypoplasia, essential tremor, hyperemesis, angiosarcoma, severe combined immunodeficiency, alveolar rhabdomyosarcoma, deformity, pulmonary stenosis, dystrophy, spondylolisthesis, hyperemesis gravidarum, muscular dystrophy, plagiocephaly, teratoma, hemiplegia, anencephaly, cardiomyopathy, amyloidosis, myasthenia gravis, epilepsy, cerebri, congenital anomaly, prosopagnosia, neurofibromas, dysgenesis, idiopathic thrombocytopenic purpura, lacunar, congenital, alopecia areata, nephritis, kyphosis, pyelonephritis, ichthyosis, choriocarcinoma, molar pregnancy, microtia, microcephaly, quadriplegia, dysphasia, hypertrophic cardiomyopathy, phenylketonuria, glomerulonephritis, otosclerosis, myotonic muscular dystrophy, enteropathy, juvenile diabetes, diabetes insipidus, astrocytoma, epididymitis, kawasaki disease, apert, eosinophilic