Source: INFERRED
CUI | Disease | Type | Disease Class | Semantic type | DO Class | HPO Term | Num. genes |
---|---|---|---|---|---|---|---|
C1834339 | Myopathy, Actin, Congenital, with Excess of Thin Myofilaments | disease | Musculoskeletal Diseases; Nervous System Diseases | Disease or Syndrome | genetic disease; disease of anatomical entity; syndrome | 1 |