Hepatoerythropoietic porphyria
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| Hepatoerythropoietic porphyria | |
|---|---|
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| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | E80.2 (ILDS E80.282) |
| ICD-9-CM | 277.1 |
| OMIM | 176100 |
| DiseasesDB | 29123 |
| Patient UK | Hepatoerythropoietic porphyria |
| MeSH | D017121 |
Hepatoerythropoietic porphyria is a very rare form of hepatic porphyria caused by a disorder in both genes which code Uroporphyrinogen III decarboxylase (UROD).[1][2]:525
It has a similar presentation to porphyria cutanea tarda (PCT), but with earlier onset.[3] In classifications which define PCT type 1 as "sporadic" and PCT type 2 as "familial", hepatoerythropoietic porphyria is more similar to type 2.
See also
- Hereditary coproporphyria
- List of cutaneous conditions
- List of dental abnormalities associated with cutaneous conditions
References
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ "hepatoerythropoietic porphyria" at Dorland's Medical Dictionary
External links
- Hepatoerythropoietic porphyria at NLM Genetics Home Reference
- Hepatoerythropoietic porphyria at NIH's Office of Rare Diseases
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