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autosomal dominant nonsyndromic deafness 69 (DOID:0110590)
Alliance: disease page
Synonyms: autosomal dominant deafness 69; DCUA; DFNA69; unilateral or asymmetric congenital deafness
Alt IDs: OMIM:616697, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory