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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 30 (DOID:0110489)
Alliance: disease page
Synonyms: autosomal recessive deafness 30; DFNB30
Alt IDs: OMIM:607101, 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 mutations in the MYO3A gene on chromosome 10p12.1.

Disease References using Mouse Models (1)

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory