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Disease Ontology Browser
autosomal dominant Alport syndrome (DOID:0110032)
Alliance: disease page
Alt IDs: OMIM:104200, ORDO:88918
Definition: An Alport syndrome that has_material -basis_in heterozygous mutation in the COL4A3 gene.

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
MGI 6.15
The Jackson Laboratory