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C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.029 Achondroplasia D000130 C16.320.033 Adrenal Hyperplasia, Congenital D000312 C16.320.775 Pain Insensitivity, Congenital D000699 C16.320.070 Anemia, Hemolytic, Congenital D000745 + C16.320.080 Ataxia Telangiectasia D001260 C16.320.170 Cherubism D002636 C16.320.190 Cystic Fibrosis D003550 C16.320.365 Hemoglobinopathies D006453 + C16.320.480 Kartagener Syndrome D007619 C16.320.540 Marfan Syndrome D008382 C16.320.565 Metabolism, Inborn Errors D008661 + C16.320.700 Neoplastic Syndromes, Hereditary D009386 + C16.320.737 Osteogenesis Imperfecta D010013 C16.320.850 Skin Diseases, Genetic D012873 + C16.320.925 Werner Syndrome D014898 C16.320.290 Eye Diseases, Hereditary D015785 + C16.320.400 Heredodegenerative Disorders, Nervous System D020271 + C16.320.590 Myasthenic Syndromes, Congenital D020294 C16.320.160 Cardiomyopathy, Hypertrophic, Familial D024741 C16.320.180 Chromosome Disorders D025063 + C16.320.099 Blood Coagulation Disorders, Inherited D025861 + C16.320.077 Anemia, Hypoplastic, Congenital D029502 + C16.320.455 Jervell-Lange Nielsen Syndrome D029593 C16.320.800 Romano-Ward Syndrome D029597 C16.320.355 Hajdu-Cheney Syndrome D031845 C16.320.322 Genetic Diseases, X-Linked D040181 +