ALAD, aminolevulinate dehydratase, 210

N. diseases: 135; N. variants: 8
Disease: Porphyrias, Hepatic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162533
Disease: Porphyrias, Hepatic
Porphyrias, Hepatic 		0.500 Biomarker group CTD_human Hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytes. 1905639 1991
CUI: C0162533
Disease: Porphyrias, Hepatic
Porphyrias, Hepatic 		0.500 Biomarker group CTD_human Enzymatic defect in a child with hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: immunochemical studies. 3684400 1987
CUI: C0162533
Disease: Porphyrias, Hepatic
Porphyrias, Hepatic 		0.500 Biomarker group RGD Mechanism of hexachlorobenzene-induced porphyria in rats. Effect of phenobarbitone pretreatment. 6721832 1984