degenerative disorder, genetic disorder, genetic defect, blastoma, becker muscular dystrophy, galactosemia, metabolic disorder, genetic abnormality, myotonic muscular dystrophy, autosomal dominant disorder, myotonia, von willebrand, monozygotic twin, embryonal rhabdomyosarcoma, parathyroid gland, neurofibromas, dystrophy, dysgenesis, achondroplasia, epilepsy, electrical conduction, monogenic, essential tremor, demyelination, cerebri, lymphoblastic leukemia, achalasia, diaphragmatic hernia, osteogenesis imperfecta, severe combined immunodeficiency, dpp, immunodeficiency, hemolytic anemia, heterotaxy, hyperinsulinism, osteogenic sarcoma, myelination, meningeal, lymphocytic leukemia, teratoma, rhabdomyosarcoma, thymosin, immunopathology, haematopoietic, neuromuscular junction, mosaicism, myelopathy, glomerulonephritis, achromatopsia, osteopetrosis, pyloric stenosis, familial hypercholesterolemia, autosomal recessive disease, sensory neuron, alveolar rhabdomyosarcoma, ethosuximide, myelomeningocele, myasthenia gravis, dyskinetic, alkalosis, autoimmunity, intraventricular, phenylketonuria, inosine, nonhereditary, gene mutation, cardiac insufficiency, chorea, malignant hyperthermia, medulloblastoma, neurogenic, anemias, chromosomal anomaly, cholestasis, adrenal insufficiency, pernicious anemia, neurotransmission, neuromotor, hyperparathyroidism, hemophilia b, hydrops, parkinsonism, motoneurons, catecholamine, neuroendocrine, eoe, thyrotoxicosis, genetic mutation, bullous, carcinoid, nephritis, idiopathic thrombocytopenic purpura, amyloidosis, hyperalgesia, erythropoiesis, hemochromatosis, neurofibromatosis, mutation, lymphocytic, dysrhythmia, factor xiii, dysphonia