FECH, ferrochelatase, 2235

N. diseases: 88; N. variants: 25
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162533
Disease: Porphyrias, Hepatic
Porphyrias, Hepatic
0.210 GeneticVariation group LHGDN Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias. 14669009 2004
CUI: C0162533
Disease: Porphyrias, Hepatic
Porphyrias, Hepatic
0.210 Biomarker group RGD Mechanism of hexachlorobenzene-induced porphyria in rats. Effect of phenobarbitone pretreatment. 6721832 1984