porphyria cutanea tarda
Information
- Disease name
- porphyria cutanea tarda
- Disease ID
- DOID:3132
- Description
- "An acute porphyria characterized by painful, blistering skin lesions that develop on sun-exposed skin." [url:http\://en.wikipedia.org/wiki/Porphyria_cutanea_tarda, url:https\://www.rarediseases.org/rare-disease-information/rare-diseases/byID/321/viewAbstract]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00005103 | Completed | Study of the Pathogenesis of Porphyria Cutanea Tarda | November 2000 | ||
| NCT00213772 | Completed | Risk Factors of Porphyria Cutanea Tarda (PCT) | May 1999 | ||
| NCT00599326 | Completed | Phase 3 | Pilot Trial of Deferasirox in the Treatment of Porphyria Cutanea Tarda | January 2008 | April 2010 |
| NCT01573754 | Completed | Phase 2 | Hydroxychloroquine and Phlebotomy for Treating Porphyria Cutanea Tarda | March 21, 2006 | July 6, 2021 |
| NCT03118674 | Completed | Phase 2 | Harvoni Treatment Porphyria Cutanea Tarda | September 6, 2017 | March 4, 2022 |
| NCT01284946 | Unknown status | Phase 2 | Safety and Efficacy of Oral Deferasirox in Patients With Porphyria Cutanea Tarda | January 2011 | December 2012 |
- Disase is a (Disease Ontology)
- DOID:3133
- Cross Reference ID (Disease Ontology)
- GARD:7433
- Cross Reference ID (Disease Ontology)
- ICD10CM:E80.1
- Cross Reference ID (Disease Ontology)
- MESH:D017119
- Cross Reference ID (Disease Ontology)
- MIM:176090
- Cross Reference ID (Disease Ontology)
- MIM:176100
- Cross Reference ID (Disease Ontology)
- NCI:C27725
- Cross Reference ID (Disease Ontology)
- ORDO:101330
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:61860000
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0162566
- OrphaNumber from OrphaNet (Orphanet)
- 101330
- MedGen concept unique identifier (MedGen Concept name)
- C0162566
- MedGen unique identifier (MedGen Concept name)
- 56453
- ICD10 preferred id (Insert disease from ICD10)
- D0003922
- ICD10 class code (Insert disease from ICD10)
- E80.1
- MeSH unique ID (MeSH (Medical Subject Headings))
- D017119