autosomal recessive nonsyndromic deafness 68

Term ID

DOID:0110519

Synonyms

• autosomal recessive deafness 68
• DFNB68

Definition

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the S1PR2 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/26805784

References

• ICD10CM:H90.3
• OMIM:610419

Ontology

Human Disease   ( DOID:0110519 )