About   Help   FAQ
Disease Ontology Browser
congenital nystagmus 1 (DOID:0111790)
Alliance: disease page
Synonyms: congenital motor nystagmus 1; NYS1; X-linked infantile nystagmus 1
Alt IDs: OMIM:310700
Definition: A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2.

Disease References using Mouse Models (1)
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
11/05/2024
MGI 6.24 		The Jackson Laboratory