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MeSH Tree Location(s) for Porphyria, Variegate

Scope Note:
An autosomal dominant porphyria that is due to a deficiency of protoporphyrinogen oxidase (EC 1.3.3.4) in the LIVER, the seventh enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include both neurological symptoms and cutaneous lesions. Patients excrete increased levels of porphyrin precursors, COPROPORPHYRINS and protoporphyrinogen.


Location corresponding to Mesh Number C06.552.830.625

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Variegate   Porphyria variegata
Location corresponding to Mesh Number C16.320.565.708.400.625

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Variegate   Porphyria variegata
Location corresponding to Mesh Number C16.320.850.742.625

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Variegate   Porphyria variegata
Location corresponding to Mesh Number C17.800.827.742.625

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Variegate   Porphyria variegata
Location corresponding to Mesh Number C17.800.849.617.400.625

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Variegate   Porphyria variegata
Location corresponding to Mesh Number C18.452.648.708.400.625

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Variegate   Porphyria variegata
Location corresponding to Mesh Number C18.452.811.400.625

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Variegate   Porphyria variegata
Location corresponding to Mesh Number C18.452.880.617.400.625

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria, Variegate   Porphyria variegata
MeSH Start Page
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