About   Help   FAQ
Disease Ontology Browser
retinitis pigmentosa 88 (DOID:0112145)
Alliance: disease page
Synonyms: RP88
Alt IDs: OMIM:618826
Definition: A retinitis pigmentosa characterized by night blindness and constriction of peripheral visual fields, with mildly reduced visual acuity that has_material_basis_in homozygous or compound heterozygous mutation in the RP1L1 gene on chromosome 8p23.1.


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
02/13/2024
MGI 6.23
The Jackson Laboratory