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© May 2005 Lorentz JÄNTSCHI && Sorana Daniela BOLBOACĂ

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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