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autosomal recessive nonsyndromic deafness 32 (DOID:0110491)
Alliance: disease page
Synonyms: autosomal recessive deafness 32; autosomal recessive deafness 105; DFNB32
Alt IDs: OMIM:608653, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, DOID:0110466, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in variation in the chromosome region 1p22.1-p13.3.


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
02/18/2020
MGI 6.14
The Jackson Laboratory