Disease: Deficiency of monooxygenase ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1291314
Disease: Deficiency of monooxygenase
Deficiency of monooxygenase 		0.010 GeneticVariation disease BEFREE Mutations in CYP27B1 cause 1α-hydroxylase deficiency, also known as vitamin D dependent rickets type I or hereditary pseudo-vitamin D deficient rickets; very rare mutations in CYP2R1 can cause 25-hydroxylase deficiency. 27060335 2017