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Disease Ontology Browser
autosomal recessive Alport syndrome (DOID:0110033)
Alliance: disease page
Alt IDs: OMIM:203780, ORDO:88919
Definition: An Alport syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the COL4A3 or the COL4A4 gene, both of which map to chromosome 2q.

Disease References using Mouse Models (20)

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 6.20
The Jackson Laboratory