RS111033270 CDH23
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What This Variant Does
"Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D....
Associated Conditions
Usher syndrome type 1D
Pituitary adenoma 5
multiple types
Autosomal recessive nonsyndromic hearing loss 12
Rare genetic deafness
Retinal dystrophy
Usher syndrome type 1
Childhood onset hearing loss
Usher syndrome
Inborn genetic diseases
CDH23-related disorder
Usher syndrome type 1D
Pituitary adenoma 5
multiple types
Autosomal recessive nonsyndromic hearing loss 12
Other Variants in CDH23