hydrops, lactase deficiency, autosomal recessive disease, severe combined immunodeficiency, monozygotic twin, phenylketonuria, lichen planus, osteopetrosis, myotonic dystrophy, rh incompatibility, myelomeningocele, puerperal psychosis, anemias, cerebri, pernicious anemia, achromatopsia, orchitis, allergic eczema, cholestasis, torticollis, hyperparathyroidism, thyroiditis, hamartoma, hyperemesis, chromosomal anomaly, pyloric stenosis, myotonia, genetic defect, fibroma, diaphragmatic hernia, rh factor, valvular heart disease, neuromotor, roseola, hyperinsulinism, degenerative disorder, lymphocytic leukemia, histiocytosis, esophageal reflux, familial hypercholesterolemia, autosomal dominant disorder, thrombocytosis, epididymitis, hemolytic, achalasia, generalized epilepsy, metaplasia, diabetes insipidus, sarcoid, toxoplasma, pyelonephritis, molar pregnancy, factor xiii, enteropathy, polydactylism, nephritis, genetic abnormality, dysgenesis, leydig cell, metabolic disorder, anosognosia, thyrotoxicosis, hydrocephaly, dysphasia, immunodeficiency, heterotaxy, neurofibromas, haemolytic anemia, mosaicism, laryngospasm, lymphocytic, malabsorption, adenomyosis, adrenal insufficiency, hemochromatosis, xeroderma pigmentosum, epiglottitis, seborrhea, osteogenesis imperfecta, superior mesenteric artery, bicuspid valve, toxemia, hyperacidity, sequela, atopic eczema, hypochondriasis, malignant hyperthermia, hypocalcaemia, herpes encephalitis, iddm, nephrosis, esotropia, bulbar, molluscum contagiosum, alveolar rhabdomyosarcoma, atresia, erythema nodosum, angiosarcoma, syngeneic, intracerebral, hemolytic anemia, oesophagitis, diabetes, myasthenia, rickets, cretinism, hemophilia, hypogonadism, insipidus, mellitus, myopathies, myxedema, porphyria, anaphylaxis, glomerulonephritis, goiter, gravis, hypoparathyroidism