Bothnia retinal dystrophy Disease Ontology Browser

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Disease Ontology Browser

Bothnia retinal dystrophy (DOID:0050683)
Alliance: disease page
Synonyms: Vasterbotten dystrophy
Alt IDs: OMIM:607475, MESH:C564392
Definition: A fundus dystrophy that is characterized by early onset of night blindness and decreased visual acuity that progresses to blindness in early adulthood, has_material_basis_in mutation in RLBP1 gene.

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 04/09/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Rlbp1tm1Jsa/Rlbp1tm1Jsa	involves: 129X1/SvJ * C57BL/6	J:68444	View