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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 79 (DOID:0110526)
Synonyms: autosomal recessive deafness 79; DFNB79
Alt IDs: OMIM:613307, ICD10CM:H90.3, ORDO:90636
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TPRN gene on chromosome 9q34.


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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
04/18/2017
MGI 6.08
The Jackson Laboratory