Autosomal recessive nonsyndromic hearing loss 33

MONDO:0011799

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 10p11.23-q21.1.

Also known as: DFNB33, autosomal recessive deafness 33, autosomal recessive nonsyndromic deafness 33, autosomal recessive nonsyndromic deafness type 33, deafness, autosomal recessive 33

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 33 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 33 (0)

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