About   Help   FAQ
Disease Ontology Browser
congenital nystagmus 3 (DOID:0111793)
Alliance: disease page
Synonyms: autosomal dominant congenital nystagmus 3; NYS3
Alt IDs: OMIM:608345
Definition: A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 7p11.2.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory