PDIK1L, PDLIM1 interacting kinase 1 like, 149420

N. diseases: 138; N. variants: 1
Disease: Xeroderma Pigmentosum, Complementation Group D ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		0.010 Biomarker disease BEFREE We therefore consider it unlikely that either the XP-D or the XP-C DNA repair deficiency is associated with a defect in the beta subunit of casein kinase II. 1694965 1990