Disease #00415 (PCT (porphyria cutanea tarda (PCT)), OMIM:176100)
| Official abbreviation |
PCT |
| Name |
porphyria cutanea tarda (PCT) |
| OMIM ID |
176100 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
HFE, UROD |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-06-15 21:27:40 +02:00 (CEST) |
| Date last edited |
N/A |
|