Autosomal dominant nonsyndromic hearing loss 67

MONDO:0014594

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the OSBPL2 gene.

Also known as: DFNA67, OSBPL2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 67, autosomal dominant nonsyndromic deafness 67, autosomal dominant nonsyndromic deafness caused by mutation in OSBPL2, autosomal dominant nonsyndromic deafness type 67, deafness, autosomal dominant 67, deafness, autosomal dominant type 67

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