autosomal recessive nonsyndromic deafness 101

Term ID

DOID:0110462

Synonyms

autosomal recessive deafness 101
DFNB101

Definition

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32. https://www.ncbi.nlm.nih.gov/pubmed/24619944

References

ICD10CM:H90.3
MIM:615837

Ontology

Human Disease ( DOID:0110462 )

Relationships

is a type of: autosomal recessive nonsyndromic deafness

autosomal recessive nonsyndromic deafness Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models