CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0795690 Congenital omphalocele disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality disease of anatomical entity; physical disorder Abnormality of the digestive system; Abnormality of connective tissue 85 13