hereditary coproporphyria "hereditary coproporphyria porphyria" EXACT [CSP2005:1849-7674] "Hereditary coproporphyria" EXACT [MTHICD9_2006:277.1] SNOMEDCT_2010_1_31:7425008 "Coproporphyrinogen oxidase deficiency" EXACT [SNOMEDCT_2005_07_31:238055004] MSH2010_2010_02_22:D046349 "Hereditary coproporphyria (disorder)" EXACT [SNOMEDCT_2005_07_31:7425008] OMIM2009_05_01:121300 SNOMEDCT_2010_1_31:238055004 URI: http://www.ebi.ac.uk/cellline#hereditary_coproporphyria UMLS_CUI:C0162531 hepatic porphyria central nervous system disease pulmonary valve disease