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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 36 (DOID:0110494)
Synonyms: autosomal recessive deafness 36; DFNB36
Alt IDs: OMIM:609006, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36.


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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
08/08/2017
MGI 6.10
The Jackson Laboratory