erythropoietic protoporphyria Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An acute porphyria characterized by a deficiency in the enzyme ferrochelatase, leading to abnormally high levels of protoporphyrin in the tissue. (Human Disease Ontology, DOID_13270)
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Genes

1 genes associated with the disease erythropoietic protoporphyria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
FECH ferrochelatase