Familial porphyria cutanea tarda

MONDO:0008296

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

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