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autosomal recessive nonsyndromic deafness 97 (DOID:0110539)
Alliance: disease page
Synonyms: autosomal recessive deafness 97; DFNB97
Alt IDs: OMIM:616705, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MET gene on chromosome 7q31.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
01/21/2020
MGI 6.14
The Jackson Laboratory