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Metadata
ID	DOID:0110513
Name	autosomal recessive nonsyndromic deafness 61
Definition	An autosomal recessive nonsyndromic deafness that is characterized by early childhood-onset moderate to severe sensorineural hearing loss and has_material_basis_in mutation in the SLC26A5 gene on chromosome 7q22. https://pubmed.ncbi.nlm.nih.gov/24164807/, https://www.ncbi.nlm.nih.gov/pubmed/12719379
Xrefs	ICD10CM:H90.3 MIM:613865
Synonyms	autosomal recessive deafness 61 [EXACT] DFNB61 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness