autosomal recessive nonsyndromic deafness 108

Term ID

DOID:0080263

Synonyms

Definition

An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous mutation in the ROR1 gene on chromosome 1p31. https://pubmed.ncbi.nlm.nih.gov/27162350/

References

• OMIM:617654

Ontology

Human Disease   ( DOID:0080263 )