genetic disorder, myotonic dystrophy, degenerative disorder, genetic defect, osteogenesis imperfecta, pyloric stenosis, congenital disorder, phenylketonuria, autosomal dominant disorder, severe combined immunodeficiency, hyperparathyroidism, genetic abnormality, galactosemia, autoimmune disorder, aplastic anemia, leukodystrophy, lactase deficiency, hypothyroidism, autoimmune disease, idiopathic thrombocytopenic purpura, ketoacidosis, hydrops, autosomal recessive disease, idiopathic, lymphoblastic leukemia, hemolytic anemia, metabolic acidosis, acidemia, osteopetrosis, iron overload, disorder, anemias, acidosis, histiocytosis, glomerulonephritis, hyperkalemia, hemochromatosis, diabetes insipidus, neurofibromatosis, cystic fibrosis, necrotizing enterocolitis, pernicious anemia, achalasia, toxemia, nephritis, neuroblastoma, eosinophilic, neurological disorder, immunodeficiency, myotonic muscular dystrophy, toxoplasmosis, adrenal insufficiency, teratoma, purpura, autoimmune, thyroiditis, preeclampsia, myxedema, generalized epilepsy, choriocarcinoma, monogenic, familial hypercholesterolemia, pancytopenia, neurodegenerative, amyloidosis, nephrotic syndrome, anencephaly, becker muscular dystrophy, rhabdomyosarcoma, hemolytic, malabsorption, diaphragmatic hernia, kidney disease, lymphocytic leukemia, cerebral palsy, hemophilia b, lactase, pheochromocytoma, xeroderma pigmentosum, hypotonia, prosopagnosia, rh positive, blastoma, lichen planus, atresia, achondroplasia, orchitis, hyperglycaemia, essential tremor, acromegaly, chronic renal failure, gastrointestinal disorder, factor xiii, enuresis, hypertrichosis, congenital anomaly, cardiomyopathy, myopathy, mody, mosaicism, cerebri, hypoplasia