degenerative disorder, metabolic disorder, congenital disorder, genetic defect, neurological disorder, genetic abnormality, myotonic dystrophy, osteogenesis imperfecta, genetic mutation, muscular dystrophy, neurofibromatosis, neuroblastoma, birth defect, gene mutation, rhabdomyosarcoma, cystic fibrosis, polycystic kidney disease, cerebral palsy, dwarfism, aplastic anemia, autoimmune disease, leukodystrophy, autoimmune disorder, duchenne, chromosomal anomaly, leukemia, epilepsy, achondroplasia, autosomal dominant disorder, disorder, spina bifida, progeria, severe combined immunodeficiency, blastoma, acute lymphoblastic leukemia, achromatopsia, retinitis pigmentosa, histiocytosis, juvenile diabetes, hemochromatosis, congenital, ataxia, phenylketonuria, dystrophy, retinoblastoma, malformation, lymphoblastic leukemia, hydrocephalus, diaphragmatic hernia, microcephaly, mutation, spastic paralysis, xeroderma pigmentosum, galactosemia, polydactylism, autosomal recessive disease, myasthenia gravis, becker muscular dystrophy, trisomy, prosopagnosia, sickle cell anemia, recessive gene, myotonic muscular dystrophy, teratoma, juvenile rheumatoid arthritis, hemolytic anemia, kidney disease, cardiomyopathy, osteopetrosis, apraxia, deafness, pyloric stenosis, disease, osteogenic sarcoma, iron overload, dysgenesis, medulloblastoma, idiopathic, syringomyelia, hydrops, alopecia areata, neurofibroma, acute myeloid leukemia, essential tremor, anencephaly, embryonal rhabdomyosarcoma, degenerative, hypotonia, congenital anomaly, pulmonary stenosis, cerebri, mental retardation, alveolar rhabdomyosarcoma, amyloidosis, myelomeningocele, hypertrichosis, kawasaki disease, dyslexia, nephritis, mutant gene, autism, alopecia

abetalipoproteinemia, albers-schonberg disease, autosomal dominant disease, chondrodystrophy, fallot's tetralogy, fibrocystic disease of the pancreas, gaucher's disease, hypobetalipoproteinemia, juvenile amaurotic idiocy, maple syrup urine disease, marble bones disease, mcardle's disease, mucovioscidosis, nanism, pancreatic fibrosis, porphyria, spielmeyer-vogt disease, tetralogy of fallot

congenital disease, genetic disease, inherited disease, inherited disorder