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 |