PomBase home

Disease association ontology term - MONDO:0010915 - autosomal dominant nonsyndromic hearing loss 4A

Term summary

ID
MONDO:0010915
Name
autosomal dominant nonsyndromic hearing loss 4A
Ontology or CV name
Disease association
Definition
Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH14 gene.

Parents

Annotation

Disease association

MONDO:0010915 - autosomal dominant nonsyndromic hearing loss 4A

References:

Genes: