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Biological Sciences and Healthcare, part 2

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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Familial porphyria cutanea tarda
... > Clinical finding (finding) > Skin AND/OR mucosa finding (finding) > Skin finding > Disease of skin > Porphyria cutanea tarda > Familial porphyria cutanea tarda
... > Clinical finding (finding) > Integumentary system finding > Skin finding > Disease of skin > Porphyria cutanea tarda > Familial porphyria cutanea tarda
... > Clinical finding (finding) > disease > Disorder of body system > Disorder of integument > Disease of skin AND/OR subcutaneous tissue > Disease of skin > Porphyria cutanea tarda > Familial porphyria cutanea tarda
... > Clinical finding (finding) > Integumentary system finding > Disorder of integument > Disease of skin AND/OR subcutaneous tissue > Disease of skin > Porphyria cutanea tarda > Familial porphyria cutanea tarda
... > Clinical finding (finding) > disease > Metabolic disease > Disorder of porphyrin metabolism > Uroporphyrinogen decarboxylase deficiency > Porphyria cutanea tarda > Familial porphyria cutanea tarda

Preferred term

Familial porphyria cutanea tarda  

Type

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

Broader concept

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URI

http://www.irandoc.acir/onto/irandoc/59229005

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