All diseases

OMIM ID
177000
OMIM term:
PROTOPORPHYRIA, ERYTHROPOIETIC; EPP
Alternative terms:
ERYTHROHEPATIC PROTOPORPHYRIA
HEME SYNTHETASE DEFICIENCY
FERROCHELATASE DEFICIENCY
(∗) Location:
18q21.31  
(†) Associated OMIM genes:
FECH  
(‡) Associated MGI genes:
Abcg2   Fech  

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