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C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.131 Abnormalities D000013 + C16.131.260 Chromosome Disorders D025063 + C16.131.260.080 Beckwith-Wiedemann Syndrome D001506 C16.131.260.190 Cri-du-Chat Syndrome D003410 C16.131.260.210 De Lange Syndrome D003635 C16.131.260.260 Down Syndrome D004314 C16.131.260.700 Prader-Willi Syndrome D011218 C16.131.260.790 Rubinstein-Taybi Syndrome D012415 C16.131.260.380 Holoprosencephaly D016142 C16.131.260.040 Angelman Syndrome D017204 C16.131.260.940 WAGR Syndrome D017624 C16.131.260.970 Williams Syndrome D018980 C16.131.260.090 Branchio-Oto-Renal Syndrome D019280 C16.131.260.800 Sex Chromosome Disorders D025064 +
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.180 Chromosome Disorders D025063 + C16.320.180.080 Beckwith-Wiedemann Syndrome D001506 C16.320.180.190 Cri-du-Chat Syndrome D003410 C16.320.180.210 De Lange Syndrome D003635 C16.320.180.260 Down Syndrome D004314 C16.320.180.700 Prader-Willi Syndrome D011218 C16.320.180.790 Rubinstein-Taybi Syndrome D012415 C16.320.180.380 Holoprosencephaly D016142 C16.320.180.040 Angelman Syndrome D017204 C16.320.180.940 WAGR Syndrome D017624 C16.320.180.970 Williams Syndrome D018980 C16.320.180.090 Branchio-Oto-Renal Syndrome D019280 C16.320.180.800 Sex Chromosome Disorders D025064 +