All diseases

OMIM ID
176200
OMIM term:
PORPHYRIA VARIEGATA
Alternative terms:
VARIEGATE PORPHYRIA; VP
PORPHYRIA, SOUTH AFRICAN TYPE
PROTOPORPHYRINOGEN OXIDASE DEFICIENCY
PPOX DEFICIENCY VARIEGATE PORPHYRIA, HOMOZYGOUS VARIANT
(∗) Location:
1q23.3   6p22.2  
(†) Associated OMIM genes:
HFE   PPOX  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/t69xg1p7