Autosomal recessive nonsyndromic hearing loss 38

MONDO:0011991

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 6q26-q27.

Also known as: DFNB38, autosomal recessive deafness 38, autosomal recessive nonsyndromic deafness 38, autosomal recessive nonsyndromic deafness type 38, deafness, autosomal recessive 38

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 38 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 38 (0)

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