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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 1 (DOID:0110541)
Alliance: disease page
Synonyms: autosomal dominant deafness 1; autosomal dominant deafness 1, with or without thrombocytopenia; DFNA1; hereditary low frequency hearing loss 1; Konigsmark syndrome; LFHL1
Alt IDs: OMIM:124900, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has_material_basis_in mutation in the DIAPH1 gene on chromosome 5q31.

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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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11/12/2024
MGI 6.24 		The Jackson Laboratory