PRX, periaxin, 57716

N. diseases: 75; N. variants: 21
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009691
Disease: Congenital cataract
Congenital cataract
0.300 Biomarker disease GENOMICS_ENGLAND Identification of a PRX variant in a Chinese family with congenital cataract by exome sequencing. 27081207 2016