Source: CLINVAR
CUI | Disease | Type | Disease Class | Semantic type | DO Class | HPO Term | Num. genes | Num. SNPs |
---|---|---|---|---|---|---|---|---|
C1861065 | CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 | disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | Disease or Syndrome | disease of anatomical entity | 2 | 7 |