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autosomal dominant nonsyndromic deafness 15

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the POU4F3 gene.
Uniprot Description A form of non-syndromic hearing loss with variable phenotype in terms of age at onset, levels of progression, and shape of audiograms.
Mondo Term and Equivalent IDs
MONDO:0011226:  autosomal dominant nonsyndromic deafness 15
MESH:C566545: 
UMLS:C1865366: