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Biological Sciences and Healthcare, part 5

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... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Erythropoietic protoporphyria > Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of porphyrin metabolism > Ferrochelatase deficiency > Erythropoietic protoporphyria > Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
... > Clinical finding (finding) > disease > Metabolic disease > Enzymopathy > Ferrochelatase deficiency > Erythropoietic protoporphyria > Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
... > Clinical finding (finding) > disease > Congenital disease > Inborn error of metabolism > Erythropoietic protoporphyria > Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
... > Clinical finding (finding) > disease > Metabolic disease > Inborn error of metabolism > Erythropoietic protoporphyria > Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Inborn error of metabolism > Erythropoietic protoporphyria > Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2

Preferred term

Erythropoietic protoporphyria due to gain of function of erythroid-specific aminolevulinic acid synthase 2  

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  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

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http://www.irandoc.acir/onto/irandoc/1186810009

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