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Disease Ontology Browser
nephrotic syndrome type 5 (DOID:0080380)
Alliance: disease page
Synonyms: nephrotic syndrome type 5, with or without ocular abnormalities
Alt IDs: OMIM:614199
Definition: A familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has_material_basis_in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p.


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)
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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory