Gene: PRH2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5555
Gene Symbol: PRH2
PRH2 		0.010 GeneticVariation disease BEFREE We report a child with thalamic infarcts due to internal CVT who had congenital heterozygous protein-C deficiency, factor V G 1691 A and A 4070 G mutations. 10876830 2000