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MeSH Tree Location(s) for Porphyria Cutanea Tarda

Scope Note:
An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.


Location corresponding to Mesh Number C06.552.830.250

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria Cutanea Tarda   Porphyria cutanea tarda
Location corresponding to Mesh Number C16.320.565.708.400.250

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria Cutanea Tarda   Porphyria cutanea tarda
Location corresponding to Mesh Number C16.320.850.742.250

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria Cutanea Tarda   Porphyria cutanea tarda
Location corresponding to Mesh Number C17.800.827.742.250

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria Cutanea Tarda   Porphyria cutanea tarda
Location corresponding to Mesh Number C17.800.849.617.400.250

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria Cutanea Tarda   Porphyria cutanea tarda
Location corresponding to Mesh Number C18.452.648.708.400.250

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria Cutanea Tarda   Porphyria cutanea tarda
Location corresponding to Mesh Number C18.452.811.400.250

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria Cutanea Tarda   Porphyria cutanea tarda
Location corresponding to Mesh Number C18.452.880.617.400.250

Porphyrias, Hepatic  Porfyri, hepatisk
Hepatisk porfyri
Porphyria Cutanea Tarda   Porphyria cutanea tarda
MeSH Start Page
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