Disease #02183

Official abbreviation XLEPP
Name protoporphyria, erythropoietic, X-linked (XLEPP)
OMIM ID 300752
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ALAS2
Associated tissues -
Disease features X-linked
Remarks -