Library Powered by BSD http://bsd.org/ FreeBSD http://freebsd.org/ MySQL http://mysql.com/ Apache http://apache.org/ PHP http://php.net/ PHP http://SourceForge.net/
© May 2005 Lorentz JÄNTSCHI && Sorana Daniela BOLBOACĂ

up one level Up

All

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.565 Metabolism, Inborn Errors D008661 + C16.320.565.066 Amino Acid Metabolism, Inborn Errors D000592 + C16.320.565.066.102 Albinism D000417 + C16.320.565.066.187 Alkaptonuria D000474 C16.320.565.066.210 Aminoaciduria, Renal D000608 + C16.320.565.066.470 Homocystinuria D006712 C16.320.565.066.608 Maple Syrup Urine Disease D008375 C16.320.565.066.620 Multiple Carboxylase Deficiency D009100 + C16.320.565.066.766 Phenylketonurias D010661 + C16.320.565.066.480 Hyperhomocysteinemia D020138 C16.320.565.066.477 Hyperglycinemia, Nonketotic D020158 C16.320.565.066.340 Citrullinemia D020159 C16.320.565.066.475 Hyperargininemia D020162 C16.320.565.066.729 Ornithine Carbamoyltransferase Deficiency Disease D020163 C16.320.565.066.275 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165 C16.320.565.066.544 Hyperlysinemias D020167 C16.320.565.066.880 Tyrosinemias D020176
C18 Nutritional and Metabolic Diseases D009750 + C18.452 Metabolic Diseases D008659 + C18.452.648 Metabolism, Inborn Errors D008661 + C18.452.648.066 Amino Acid Metabolism, Inborn Errors D000592 + C18.452.648.066.102 Albinism D000417 + C18.452.648.066.187 Alkaptonuria D000474 C18.452.648.066.210 Aminoaciduria, Renal D000608 + C18.452.648.066.470 Homocystinuria D006712 C18.452.648.066.608 Maple Syrup Urine Disease D008375 C18.452.648.066.620 Multiple Carboxylase Deficiency D009100 + C18.452.648.066.766 Phenylketonurias D010661 + C18.452.648.066.480 Hyperhomocysteinemia D020138 C18.452.648.066.477 Hyperglycinemia, Nonketotic D020158 C18.452.648.066.340 Citrullinemia D020159 C18.452.648.066.475 Hyperargininemia D020162 C18.452.648.066.729 Ornithine Carbamoyltransferase Deficiency Disease D020163 C18.452.648.066.275 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165 C18.452.648.066.544 Hyperlysinemias D020167 C18.452.648.066.880 Tyrosinemias D020176