Autosomal recessive nonsyndromic hearing loss 8

MONDO:0010987

An autosomal recessive nonsyndromic deafness that has material basis in mutation in the TMPRSS3 gene on chromosome 21q22.

Also known as: autosomal recessive nonsyndromic hearing loss 8, DFNB10, DFNB8, NRSD8, autosomal recessive deafness 10, autosomal recessive deafness 8, autosomal recessive nonsyndromic deafness 8, autosomal recessive nonsyndromic deafness type 8

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 8 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 8 (0)

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