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Disease Ontology Browser
autosomal recessive Alport syndrome (DOID:0110033)
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 (17)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory