RS111033271 CDH23
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What This Variant Does
"CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome an...
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 12
Rare genetic deafness
Usher syndrome type 2A
Usher syndrome type 1
Usher syndrome
Pituitary adenoma 5
multiple types
Usher syndrome type 1D
CDH23-related disorder
Retinal dystrophy
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 12
Rare genetic deafness
Usher syndrome type 2A
Usher syndrome type 1
Other Variants in CDH23