Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 64072
  • Symbol: CDH23
  • Description: cadherin related 23

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Disease_Term Source Rank Other Values
Deafness, autosomal recessive 12, 601386 (3) OMIM high
  • Genome region : 10q22.1
  • OMIM_ID : 601386 OMIM phenotype ID
  • OMIM_ID : 605516 OMIM gene ID
Usher syndrome, type 1D/F digenic, 601067 (3) OMIM high
  • Genome region : 10q21.1
  • Genome region : 10q22.1
  • OMIM_ID : 601067 OMIM phenotype ID
  • OMIM_ID : 605514 OMIM gene ID
  • OMIM_ID : 605516 OMIM gene ID
Usher syndrome, type 1D, 601067 (3) OMIM high
  • Genome region : 10q22.1
  • OMIM_ID : 601067 OMIM phenotype ID
  • OMIM_ID : 605516 OMIM gene ID
Diisocyanate-induced asthma GWAS high
Vitiligo GWAS high
Age at smoking initiation in chronic obstructive pulmonary disease GWAS high
Kidney function decline traits GWAS high
Bipolar disorder (body mass index interaction) GWAS high