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bn:02945169n
Noun Concept
Categories: Porphyrias, Heme metabolism disorders
EN
harderoporphyria
EN
Harderoporphyria is a rare disorder of heme biosynthesis, inherited in an autosomal recessive manner caused by specific mutations in the CPOX gene. Wikipedia
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Sources
EN
Harderoporphyria is a rare disorder of heme biosynthesis, inherited in an autosomal recessive manner caused by specific mutations in the CPOX gene. Wikipedia
medical condition Wikidata
IS A
porphyria
Wikipedia
EN
harderoporphyria
Wikidata
EN
Harderoporphyria

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