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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
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