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C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.614 Infant, Newborn, Diseases D007232 + C16.614.042 Amniotic Band Syndrome D000652 C16.614.053 Anemia, Neonatal D000751 + C16.614.092 Asphyxia Neonatorum D001238 C16.614.131 Birth Injuries D001720 + C16.614.213 Cystic Fibrosis D003550 C16.614.304 Erythroblastosis, Fetal D004899 + C16.614.378 Hemorrhagic Disease of Newborn D006475 C16.614.390 Hernia, Umbilical D006554 C16.614.414 Hydrocephalus D006849 + C16.614.438 Hydrophthalmos D006871 C16.614.465 Hyperostosis, Cortical, Congenital D006958 C16.614.492 Ichthyosis D007057 + C16.614.521 Infant, Premature, Diseases D007235 + C16.614.555 Jaundice, Neonatal D007567 C16.614.580 Meconium Aspiration D008471 C16.614.610 Neonatal Abstinence Syndrome D009357 C16.614.677 Ophthalmia Neonatorum D009878 C16.614.694 Persistent Fetal Circulation Syndrome D010547 C16.614.739 Poikiloderma Congenitale D011038 C16.614.810 Sclerema Neonatorum D012593 C16.614.868 Syphilis, Congenital D013590 C16.614.890 Thanatophoric Dysplasia D013796 C16.614.909 Toxoplasmosis, Congenital D014125 C16.614.947 Wolman Disease D015223 C16.614.815 Severe Combined Immunodeficiency D016511 C16.614.595 Mobius Syndrome D020331 C16.614.643 Nystagmus, Congenital D020417 C16.614.258 Epilepsy, Benign Neonatal D020936 C16.614.716 Persistent Hyperinsulinemia Hypoglycemia of Infancy D044903