loading...| Preferred Name |
炎性多神经病 / Inflammatory polyneuropathy |
| Definitions |
Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guillain-Barré syndrome) with the motor deficit reaching a maximal level by 28 days, and chronic inflammatory demyelinating polyneuropathy (CIDP) which has a slowly progressive course of two or more months or a relapsing remitting course. There are many variants of AIDP and CIDP. |
| ID |
http://purl.bmicc.cn/ontology/ICD11CN/8C01 |
| definition |
Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guillain-Barré syndrome) with the motor deficit reaching a maximal level by 28 days, and chronic inflammatory demyelinating polyneuropathy (CIDP) which has a slowly progressive course of two or more months or a relapsing remitting course. There are many variants of AIDP and CIDP. |
| hasDbXref | |
| label |
炎性多神经病 / Inflammatory polyneuropathy |
| mappingRelation | |
| notation |
8C01 |
| prefixIRI |
ICD11CN:C01 |
| prefLabel |
炎性多神经病 / Inflammatory polyneuropathy |
| subClassOf |