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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 4B (DOID:0110574)
Synonyms: autosomal dominant deafness 4B; DFNA4B
Alt IDs: OMIM:614614, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13.


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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
06/20/2017
MGI 6.10
The Jackson Laboratory