familial hypercholesterolemia, galactosemia, lactase deficiency, pku, metabolic disorder, atopic eczema, factor xiii, dihydrochloride, anemias, exocrine, phenylalanine, thyrotoxicosis, erythematosus, degenerative disorder, hypoparathyroidism, plaquenil, myotonic dystrophy, nephrotic syndrome, cheilitis, severe combined immunodeficiency, hypocalcaemia, heterotaxy, idiopathic thrombocytopenic purpura, osteomalacia, hyperbilirubinemia, neurofibromas, hypercalciuria, griseofulvin, mody, hypercalcemia, generalized epilepsy, bacteriuria, hypersensitivity reaction, pyloric stenosis, xeroderma pigmentosum, neurogenic bladder, lichen planus, blepharospasm, leflunomide, nitrofurantoin, secondary amenorrhea, tinea capitis, hyperparathyroidism, seborrhea, pyridoxine, hyperinsulinism, hemolytic anemia, pernicious anemia, hydrops, genetic disorder, fumarate, autosomal recessive disease, cardiac glycoside, iron overload, rh positive, diaper dermatitis, molar pregnancy, lupus erythematosus, hydroxylase, hypercalcaemia, tricyclic antidepressant, pheochromocytoma, myasthenia gravis, maleate, refractory anemia, flecainide, procardia, myoclonus, monozygotic twin, adrenal insufficiency, achromatopsia, seborrheic dermatitis, salicylates, primidone, achalasia, osteogenesis imperfecta, ichthyosis, metabolic acidosis, erythema nodosum, cerebri, histiocytosis, epididymitis, thyroiditis, adenosine deaminase, dihydroergotamine, methemoglobinemia, chorionic villus sampling, acetylcholinesterase, hyperkalemia, anencephaly, genetic abnormality, sporanox, diabetes insipidus, esotropia, pyelonephritis, myelomeningocele, pulmonary stenosis, atopic, thrombocytosis, autosomal dominant disorder, monoamine oxidase inhibitor, rh factor, hyperthyroidism, mellitus, diabetes, myasthenia, glaucoma, rickets, gravis, hemochromatosis, hypothyroidism, parkinsonism, poliomyelitis, sle, coagulopathy, cretinism, epilepsy

genetic screening, pku test