You are using an outdated browser. Please upgrade your browser to improve your experience.

autosomal recessive nonsyndromic deafness 86

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the TBC1D24 gene.
Uniprot Description A form of non-syndromic deafness characterized by prelingual onset of profound sensorineural hearing loss affecting all frequencies.
Disease Ontology Description An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.
Mondo Term and Equivalent IDs
MONDO:0013826:  autosomal recessive nonsyndromic deafness 86
UMLS:C2829265: