autosomal recessive nonsyndromic deafness 13 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive nonsyndromic deafness 13 (DOID:0110468)
Alliance: disease page
Synonyms: autosomal recessive deafness 13; DFNB13
Alt IDs: OMIM:603098, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 7q34-q36.

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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