Link to this page
National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000003537
http://purl.bioontology.org/ontology/NDFRT/N0000003537
|
|---|---|
| Preferred Name | Porphyria Cutanea Tarda [Disease/Finding] |
| Synonyms |
Porphyria Cutanea Tarda
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | Porphyria Cutanea Tarda
|
|---|---|
| prefLabel | Porphyria Cutanea Tarda [Disease/Finding]
|
| notation | N0000003537
|
| May be treated by | |
| Has contraindicated drug | |
| MESH DEFINITION | An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.
|
| MESH UI | M0026011
|
| subClassOf | |
| Semantic type UMLS property | |
| MeSH name | Porphyria Cutanea Tarda
|
| NDFRT kind | DISEASE_KIND
|
| type | |
| SNOMED CID | 61860000
|
| tui | T047
|
| NUI | N0000003537
|
| cui | C0162566
|
| MESH DUI | D017119
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |