/familial porphyria cutanea tarda

familial porphyria cutanea tarda

Rare Disease

MONDO:0008296

Also Known As

hereditary porphyria cutanea tardaporphyria cutanea tarda type IIporphyria cutanea tarda, susceptibility toPCTPCT, 'familial' typePCT, type 2Urod deficiencyporphyria cutanea tardaporphyria cutanea tarda, type 2porphyria, Hepatocutaneous typeporphyria, hepatoerythropoieticuroporphyrinogen decarboxylase deficiency

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

UROD ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

Related Diseases

sporadic porphyria cutanea tarda

MONDO:0008295

Rare

hepatoerythropoietic porphyria

MONDO:0019799

Rare

← Back to All Diseases