Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64072
Gene Symbol: CDH23
CDH23
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: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Fates of Cdh23/CDH23 with mutations affecting the cytoplasmic region. 16281288

2006

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
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: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration. 14609561

2003

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. 11138008

2001

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23). 11750125

2001

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata. 11322776

2001

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Chromosomal localization of a gene responsible for vestibulocochlear defects of BUS/Idr mice: identification as an allele of waltzer. 10452381

1999

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer. 9021139

1997

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD CD1d1 mutant mice are deficient in natural T cells that promptly produce IL-4. 9133426

1997

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Cochlear histopathology of the mutant bustling mouse, BUS/Idr. 8790740

1996

Entrez Id: 64072
Gene Symbol: CDH23
CDH23
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.500 Biomarker MGD Behavioural profiles of neurological mutant mice. 5955164

1966