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autosomal recessive nonsyndromic deafness 48 (DOID:0110505)
Synonyms: autosomal recessive deafness 48; DFNB48
Alt IDs: OMIM:609439, ICD10CM:H90.3, ORDO:90636
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the CIB2 gene on chromosome 15q25.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory