Please sign in to follow a disease.

Autosomal recessive nonsyndromic hearing loss 65

MONDO:0012452

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 20q13.2-q13.3.

Also known as: DFNB65, autosomal recessive deafness 65, autosomal recessive nonsyndromic deafness 65, autosomal recessive nonsyndromic deafness type 65, deafness, autosomal recessive 65

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 65 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 65 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.