porphyria cutanea tarda Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An acute porphyria characterized by painful, blistering skin lesions that develop on sun-exposed skin. (Human Disease Ontology, DOID_3132)
External Link http://www.omim.org/entry/176100
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Genes

1 genes associated with the porphyria cutanea tarda phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
UROD uroporphyrinogen decarboxylase