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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CDH23 and autosomal recessive nonsyndromic deafness in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with CDH23 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 137 RGD objects have been annotated to autosomal recessive nonsyndromic deafness  (DOID:0050565)
  • 0 papers in RGD have been used to annotate CDH23
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive nonsyndromic deafness | ClinVar Annotator: match by term: Deafness, autosomal recessive
  • Original References(s): PMID:11090341 PMID:11138009 PMID:11857743 PMID:12075507 PMID:15353998 PMID:16199547 PMID:16679490 PMID:17407589 PMID:18429043 PMID:19683999 PMID:20513143 PMID:20613545 PMID:21436283 PMID:21569298 PMID:21940737 PMID:22899989 PMID:23804846 PMID:24033266 PMID:24498627 PMID:25404053 PMID:25741868 PMID:25963016 PMID:27018795 PMID:27573290 PMID:27792758 PMID:28492532 PMID:29148562 PMID:30303587 PMID:31445392 PMID:32485727 PMID:32645618 PMID:32842620 PMID:35020051 PMID:8894709


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