Disease: Alopecia universalis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Alopecia universalis
CUI: C0263505
Disease: Alopecia universalis
0.010 GeneticVariation BEFREE We found that AA patients are more likely to carry the PTPN22 C1858T genotype than UrCs (p = 0.075), and this association reached significance in patients with the most severe disease presentation (Alopecia universalis vs. UrC, p = 0.024). 24055692 2014