autosomal recessive nonsyndromic deafness 107

Term ID

DOID:0080262

Synonyms

Definition

An autosomal recessive nonsyndromic deafness that has_material_basis_in compound heterozygous mutation in the WBP2 gene on chromosome 17q25. https://pubmed.ncbi.nlm.nih.gov/26881968/

References

• OMIM:617639

Ontology

Human Disease   ( DOID:0080262 )