Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 494513
Gene Symbol: PJVK
PJVK
CUI: C0011053
Disease: Deafness
Deafness
0.400 Biomarker CTD_human Previous studies have described two missense mutations in the human pejvakin gene that cause nonsyndromic recessive deafness (DFNB59) by affecting the function of auditory neurons. 17329413

2007

Entrez Id: 494513
Gene Symbol: PJVK
PJVK
CUI: C0011053
Disease: Deafness
Deafness
0.400 CausalMutation CLINVAR