Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5589
Gene Symbol: PRKCSH
PRKCSH
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		0.010 Biomarker BEFREE However, no potential disease causing mutation was found and therefore the PRKCSH gene can be excluded for both FHM and EA-2. 9043864

1996