Source:http://linkedlifedata.com/resource/lhgdn/association:41767
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).
|
| lhgdn:mesh_code |
D052245
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |