Hepatoerythropoietic porphyria
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| Hepatoerythropoietic porphyria | |
 | |
|---|---|
| UroD drawn from PDB: 1URO. | |
| ICD-10 | E80.2 (ILDS E80.282) |
| ICD-9 | 277.1 |
| OMIM | 176100 |
| DiseasesDB | 29123 |
| MeSH | D017121 |
Hepatoerythropoietic porphyria is a very rare form of hepatic porphyria caused by a disorder in the gene which codes Uroporphyrinogen III decarboxylase (UROD).
It is sometimes called porphyria cutanea tarda type 2.
External links
- Hepatoerythropoietic porphyria at NLM Genetics Home Reference