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Metadata
ID	DOID:0110505
Name	autosomal recessive nonsyndromic deafness 48
Definition	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the CIB2 gene on chromosome 15q25. https://www.ncbi.nlm.nih.gov/pubmed/23023331
Xrefs	ICD10CM:H90.3 MIM:609439
Synonyms	autosomal recessive deafness 48 [EXACT] DFNB48 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness