Autosomal recessive nonsyndromic hearing loss 104

MONDO:0014675

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the RIPOR2 gene.

Also known as: DFNB104, RIPOR2 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 104, autosomal recessive nonsyndromic deafness 104, autosomal recessive nonsyndromic deafness caused by mutation in RIPOR2, autosomal recessive nonsyndromic deafness type 104, deafness, autosomal recessive 104, deafness, autosomal recessive type 104

0 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

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