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Disease Ontology Browser
X-linked Alport syndrome (DOID:0110034)
Alliance: disease page
Synonyms: nephropathy and deafness, X-linked
Alt IDs: OMIM:301050, ORDO:88917
Definition: An Alport syndrome that has_material_basis_in mutation in the gene encoding the alpha-5 chain of basement membrane collagen type IV (COL4A5).

Disease References using Mouse Models (2)

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
12/03/2019
MGI 6.14
The Jackson Laboratory