All diseases

OMIM ID
176100
OMIM term:
PORPHYRIA CUTANEA TARDA
Alternative terms:
PCT
PORPHYRIA CUTANEA TARDA, TYPE II
PCT, TYPE II
PCT, 'FAMILIAL' TYPE
PORPHYRIA, HEPATOCUTANEOUS TYPE
UROPORPHYRINOGEN DECARBOXYLASE DEFICIENCY
UROD DEFICIENCY PORPHYRIA, HEPATOERYTHROPOIETIC, INCLUDED; HEP, INCLUDED
(∗) Location:
1p34.1   6p22.2  
(†) Associated OMIM genes:
HFE   UROD  
(‡) Associated MGI genes:

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