Jump to:
loading...| Preferred Name |
肌营养不良 / Muscular dystrophy |
| Definitions |
Progressive, hereditary skeletal muscle diseases characterized by muscle weakness, wasting, defects in muscle proteins, necrosis of muscle tissue and replacement of muscle tissue with connective and fatty tissue. |
| ID |
http://purl.bmicc.cn/ontology/ICD11CN/8C70 |
| Coded_Elsewhere |
Muscular dystrophy affecting extraocular muscle (9C82.1) Epidermolysis bullosa simplex with muscular dystrophy (EC30) Barth syndrome (5C50.E0) |
| definition |
Progressive, hereditary skeletal muscle diseases characterized by muscle weakness, wasting, defects in muscle proteins, necrosis of muscle tissue and replacement of muscle tissue with connective and fatty tissue. |
| free_Translation | |
| has_exact_match | |
| hasDbXref | |
| label |
肌营养不良 / Muscular dystrophy |
| notation |
8C70 |
| prefixIRI |
ICD11CN:C70 |
| prefLabel |
肌营养不良 / Muscular dystrophy |
| subClassOf |
Create New Mapping