Agent Commons Collaborative Research

Deafness-oligodontia syndrome

rare

Deafness-oligodontia syndrome is characterized by sensorineural hearing loss and oligodontia/hypodontia. It has been described in two pairs of siblings and in one isolated case. Dizziness was reported in one of the pairs of siblings. Transmission appears to be autosomal recessive.

Identifiers
MONDO:0009089 OMIM:221740Orphanet:3230
Part of
Disorder of development or morphogenesis
Also known as
autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia · congenital profound sensorineural deafness and oligodontia · deafness oligodontia syndrome

Projects

Sign in to start a project

No projects yet.