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© May 2005 Lorentz JÄNTSCHI && Sorana Daniela BOLBOACĂ

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C11 Eye Diseases D005128 + C11.270 Eye Diseases, Hereditary D015785 + C11.270.040 Albinism D000417 + C11.270.040.545 Albinism, Oculocutaneous D016115 + C11.270.040.545.400 Hermanski-Pudlak Syndrome D022861
C15 Hemic and Lymphatic Diseases D006425 + C15.378 Hematologic Diseases D006402 + C15.378.100 Blood Coagulation Disorders D001778 + C15.378.100.425 Blood Coagulation Disorders, Inherited D025861 + C15.378.100.425.515 Hermanski-Pudlak Syndrome D022861
C15 Hemic and Lymphatic Diseases D006425 + C15.378 Hematologic Diseases D006402 + C15.378.100 Blood Coagulation Disorders D001778 + C15.378.100.685 Platelet Storage Pool Deficiency D010981 + C15.378.100.685.400 Hermanski-Pudlak Syndrome D022861
C15 Hemic and Lymphatic Diseases D006425 + C15.378 Hematologic Diseases D006402 + C15.378.140 Blood Platelet Disorders D001791 + C15.378.140.735 Platelet Storage Pool Deficiency D010981 + C15.378.140.735.400 Hermanski-Pudlak Syndrome D022861
C15 Hemic and Lymphatic Diseases D006425 + C15.378 Hematologic Diseases D006402 + C15.378.463 Hemorrhagic Disorders D006474 + C15.378.463.735 Platelet Storage Pool Deficiency D010981 + C15.378.463.735.400 Hermanski-Pudlak Syndrome D022861
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.099 Blood Coagulation Disorders, Inherited D025861 + C16.320.099.515 Hermanski-Pudlak Syndrome D022861
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.290 Eye Diseases, Hereditary D015785 + C16.320.290.040 Albinism D000417 + C16.320.290.040.100 Albinism, Oculocutaneous D016115 + C16.320.290.040.100.400 Hermanski-Pudlak Syndrome D022861
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 + C16.320.565.066.102.100 Albinism, Oculocutaneous D016115 + C16.320.565.066.102.100.400 Hermanski-Pudlak Syndrome D022861
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.850 Skin Diseases, Genetic D012873 + C16.320.850.080 Albinism D000417 + C16.320.850.080.100 Albinism, Oculocutaneous D016115 + C16.320.850.080.100.400 Hermanski-Pudlak Syndrome D022861
C17 Skin and Connective Tissue Diseases D017437 + C17.800 Skin Diseases D012871 + C17.800.621 Pigmentation Disorders D010859 + C17.800.621.440 Hypopigmentation D017496 + C17.800.621.440.102 Albinism D000417 + C17.800.621.440.102.100 Albinism, Oculocutaneous D016115 + C17.800.621.440.102.100.400 Hermanski-Pudlak Syndrome D022861
C17 Skin and Connective Tissue Diseases D017437 + C17.800 Skin Diseases D012871 + C17.800.827 Skin Diseases, Genetic D012873 + C17.800.827.080 Albinism D000417 + C17.800.827.080.100 Albinism, Oculocutaneous D016115 + C17.800.827.080.100.400 Hermanski-Pudlak Syndrome D022861
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 + C18.452.648.066.102.100 Albinism, Oculocutaneous D016115 + C18.452.648.066.102.100.400 Hermanski-Pudlak Syndrome D022861