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Disease Ontology Browser
autosomal recessive nonsyndromic deafness (DOID:0050565)
Alliance: disease page
Alt IDs: OMIM:607197, ICD10CM:H90.3, OMIM:PS220290, ORDO:90636
Definition: A nonsyndromic deafness characterized by an autosomal recessive inheritance mode.

Disease References using Mouse Models (55)
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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Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory