Disease: fontaine syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0795932
Disease: fontaine syndrome
fontaine syndrome 		0.010 GeneticVariation disease BEFREE Our findings identify SLC25A24 mutations affecting codon 217 as the underlying genetic cause of human progeroid Fontaine syndrome. 29100094 2017