Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:609006 - DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT; DFNB36

Xenbase Genes: espn

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012170 - autosomal recessive nonsyndromic hearing loss 36
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110494 - autosomal recessive nonsyndromic deafness 36