Alport syndrome

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Summary

Literature (0)

DOID:10983 - Alport syndrome

Disease Ontology Definition:A monogenic disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss.

Synonyms: Hereditary Nephritis,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): monogenic disease (is_a)