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loading...| Preferred Name |
波伊茨-耶格综合征 / Peutz-Jeghers syndrome |
| Definitions |
Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder characterized by intestinal hamartomatous polyps in association with a distinct pattern of skin and mucosal macular melanin deposition. Patients have an increased risk of developing intestinal cancer. |
| ID |
http://purl.bmicc.cn/ontology/ICD11CN/LD2D.0 |
| definition |
Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder characterized by intestinal hamartomatous polyps in association with a distinct pattern of skin and mucosal macular melanin deposition. Patients have an increased risk of developing intestinal cancer. |
| hasDbXref | |
| label |
波伊茨-耶格综合征 / Peutz-Jeghers syndrome |
| mappingRelation | |
| notation |
LD2D.0 |
| prefixIRI |
ICD11CN:LD2D.0 |
| prefLabel |
波伊茨-耶格综合征 / Peutz-Jeghers syndrome |
| subClassOf |
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