genetic disorder, neurological disorder, myotonic dystrophy, autoimmune disease, essential tremor, embryonal rhabdomyosarcoma, leukodystrophy, congenital disorder, neurofibromatosis, degenerative, autoimmune disorder, genetic defect, polycystic kidney disease, blastoma, retinitis pigmentosa, metabolic disorder, achondroplasia, becker muscular dystrophy, osteogenesis imperfecta, rhabdomyosarcoma, achromatopsia, osteogenic sarcoma, syringomyelia, histiocytosis, myasthenia gravis, autosomal dominant disorder, ataxia, alveolar rhabdomyosarcoma, rheumatic disease, severe combined immunodeficiency, dystrophy, disease, osteopetrosis, galactosemia, muscular dystrophy, nephritis, retinitis, neurological, diaphragmatic hernia, spastic paralysis, xeroderma pigmentosum, lymphocytic leukemia, aplastic anemia, thyroiditis, hemolytic anemia, myelopathy, phenylketonuria, cerebral palsy, wilms tumour, multiple sclerosis, amyloidosis, angiosarcoma, lymphoblastic leukemia, dysgenesis, juvenile rheumatoid arthritis, cerebri, genetic abnormality, amyotrophic lateral sclerosis, hypotonia, epilepsy, demyelination, neuroblastoma, pernicious anemia, immunodeficiency, hydrops, generalized epilepsy, rheumatoid arthritis, bicuspid valve, gene mutation, familial hypercholesterolemia, monogenic, hemochromatosis, kawasaki disease, scleroderma, dysphasia, hemiplegia, autoimmune, myelomeningocele, scoliosis, congenital anomaly, myotonic muscular dystrophy, cystic fibrosis, autosomal recessive disease, vasculitis, neurosyphilis, acute myeloid leukemia, anosognosia, prosopagnosia, glomerulonephritis, diabetes insipidus, carcinoid, herpes encephalitis, neuritis, neurofibroma, pulmonary stenosis, cardiomyopathy, paresis, polydactylism, myotonia, acromegaly, roseola, congenital abnormality