About   Help   FAQ
Disease Ontology Browser
nephrotic syndrome type 15 (DOID:0080271)
Alliance: disease page
Alt IDs: OMIM:617609
Definition: A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the MAGI2 gene on chromosome 7q21.


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