Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 65217
Gene Symbol: PCDH15
PCDH15
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD The circling mutant Pcdh15roda is a new mouse model for hearing loss. 24044941

2014

Entrez Id: 65217
Gene Symbol: PCDH15
PCDH15
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. 18339676

2008

Entrez Id: 65217
Gene Symbol: PCDH15
PCDH15
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Inducing mutations in the mouse genome with the chemical mutagen ethylnitrosourea. 16972005

2006

Entrez Id: 65217
Gene Symbol: PCDH15
PCDH15
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD A quantitative survey of gravity receptor function in mutant mouse strains. 16235133

2005

Entrez Id: 65217
Gene Symbol: PCDH15
PCDH15
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice. 11124469

2001