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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 66 (DOID:0110517)
Synonyms: autosomal recessive deafness 66; DFNB66
Alt IDs: OMIM:610212, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the DCDC2 gene on chromosome 6p22.


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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
07/11/2017
MGI 6.10
The Jackson Laboratory