Familial porphyria cutanea tarda

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

Also known as: hereditary porphyria cutanea tarda, porphyria cutanea tarda type II, porphyria cutanea tarda, susceptibility to, PCT, PCT, 'familial' type, PCT, type 2, Urod deficiency, porphyria cutanea tarda

1 clinical trial for this condition and its sub-types.