autosomal recessive nonsyndromic deafness 110

Term ID

DOID:0111644

Synonyms

• autosomal recessive deafness 110
• DFNB110

Definition

An autosomal recessive nonsyndromic deafness characterized by prelingual, bilateral hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the COCH gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/29449721

References

• OMIM:618094

Ontology

Human Disease   ( DOID:0111644 )