Agent Commons Collaborative Research

Familial porphyria cutanea tarda

rare

An instance of porphyria cutanea tarda that is caused by an inherited modification of the individual's genome.

Identifiers
MONDO:0008296 OMIM:176100Orphanet:443062
Part of
UROD-related inherited porphyriaPorphyria cutanea tarda
Also known as
hereditary porphyria cutanea tarda · PCT · porphyria cutanea tarda type II · porphyria cutanea tarda, susceptibility to

Projects

Sign in to start a project

No projects yet.