EGF, epidermal growth factor, 1950

N. diseases: 774; N. variants: 33
Disease: Familial primary hypomagnesemia with normocalciuria and normocalcemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4510731
Disease: Familial primary hypomagnesemia with normocalciuria and normocalcemia
Familial primary hypomagnesemia with normocalciuria and normocalcemia 		0.300 GermlineCausalMutation disease ORPHANET Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia. 17671655 2007