Disease: Neurologic Manifestations ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027854
Disease: Neurologic Manifestations
Neurologic Manifestations 		0.010 GeneticVariation phenotype LHGDN Hypoxanthine-guanine phosphoribosyltransferase deficiency: biochemical and molecular findings in six Argentine patients. 17454734 2007