Autosomal recessive nonsyndromic hearing loss 49

An autosomal recessive disorder caused by mutations in the MARVELD2 gene, encoding MARVEL domain-containing protein 2. The condition is characterized by profound prelingual deafness.

Also known as: autosomal recessive nonsyndromic hearing loss 49, DFNB49, MARVELD2 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 49, autosomal recessive nonsyndromic deafness 49, autosomal recessive nonsyndromic deafness caused by mutation in MARVELD2, autosomal recessive nonsyndromic deafness type 49, deafness, autosomal recessive 49

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 49 itself.