About   Help   FAQ
Disease Ontology Browser
nephrotic syndrome type 18 (DOID:0080393)
Alliance: disease page
Alt IDs: OMIM:618177
Definition: A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42.


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
09/19/2023
MGI 6.22
The Jackson Laboratory