About   Help   FAQ
Disease Ontology Browser
cataract 39 multiple types (DOID:0110236)
Alliance: disease page
Synonyms: autosomal dominant cataract 39 multiple types; CTRCT39
Alt IDs: OMIM:615188, ICD10CM:Q12.0
Definition: A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34.

Disease References using Mouse Models (3)

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
01/24/2023
MGI 6.22
The Jackson Laboratory