About   Help   FAQ
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.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory