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autosomal recessive nonsyndromic deafness 101 (DOID:0110462)
Alliance: disease page
Synonyms: autosomal recessive deafness 101; DFNB101
Alt IDs: ICD10CM:H90.3, OMIM:615837
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32.


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
06/12/2024
MGI 6.13
The Jackson Laboratory