Alport syndrome

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Summary

Literature (0)

DOID:10983 - Alport syndrome

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

Synonyms: Hereditary Nephritis

Xenbase 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

: col4a5

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0018965 - Alport syndrome

MONDO:0018965 - Alport syndrome

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

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

Parent(s): monogenic disease (is_a), syndrome (is_a)