Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Metabolic disease
/
Inborn errors of metabolism
/
Inborn disorder of porphyrin metabolism
/
Inherited porphyria
/
CPOX-related hereditary coproporphyria
Harderoporphyria
rare
Identifiers
MONDO:0030048
OMIM:618892
Orphanet:659672
Causal genes
CPOX
Part of
CPOX-related hereditary coproporphyria
Also known as
HARPO
Projects
Sign in to start a project
No projects yet.