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autosomal recessive nonsyndromic deafness 125 (DOID:0061124)
Alliance: disease page
Synonyms: autosomal recessive deafness 125; DFNB125
Alt IDs: OMIM:620877
Definition: An autosomal recessive nonsyndromic deafness characterized by congenital nonsyndromic sensorineural hearing loss hat has_material_basis_in homozygous mutation in the GAS2 gene on chromosome 11p14.

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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03/18/2025
MGI 6.24 		The Jackson Laboratory