| Disease #01264 (HCP (coproporphyria, hereditary), OMIM:121300)
        
          | Official abbreviation | HCP |  
          | Name | coproporphyria, hereditary |  
          | OMIM ID | 121300 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal dominant, Autosomal recessive |  
          | Individuals reported having this disease | 7 |  
          | Phenotype entries for this disease | 6 |  
          | Associated with 1 gene | CPOX |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2014-09-25 23:29:40 +02:00 (CEST) |  
          | Date last edited | 2021-12-10 21:51:32 +01:00 (CET) |  
 
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