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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 98 (DOID:0110540)
Synonyms: autosomal recessive deafness 98; DFNB98
Alt IDs: OMIM:614861, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TSPEAR gene on chromosome 21q22.


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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
09/12/2017
MGI 6.10
The Jackson Laboratory