retinitis pigmentosa 59 Disease Ontology Browser

Home
Genes
Phenotypes
Human Disease
Expression
Recombinases
Function
Strains / SNPs
Homology
Tumors

About Help FAQ

Search
Download
More Resources
Submit Data
Find Mice (IMSR)
Analysis Tools
Contact Us
Browsers

Disease Ontology Browser

retinitis pigmentosa 59 (DOID:0110352)
Alliance: disease page
Synonyms: RP59
Alt IDs: OMIM:613861, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11.

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, Copyright, and Privacy Statement Send questions and comments to User Support.	last database update 01/31/2023 MGI 6.22

Allelic Composition	Genetic Background	Reference	Phenotypes
Dhddstm1.1Sjpi/Dhddstm1.1Sjpi Tg(BEST1-rtTA,tetO-cre)1Yzl/0	involves: C57BL/6J * FVB/N	J:287362	View