CUI | Disease | Type | Disease Class | Semantic type | DO Class | HPO Term | Num. genes | Num. SNPs |
---|---|---|---|---|---|---|---|---|
C0007193 | Cardiomyopathy, Dilated | group | Cardiovascular Diseases | Disease or Syndrome | genetic disease; disease of anatomical entity | Abnormality of the cardiovascular system | 43 | 443 |
C4225408 | CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25 | disease | Disease or Syndrome | disease of anatomical entity | 1 | 5 | ||
C1866008 | Muscular Dystrophy, Limb-Girdle, Type 2G | disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | Disease or Syndrome | disease of anatomical entity | 1 | 5 |