Alport syndrome Disease Ontology Browser

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Disease Ontology Browser

Alport syndrome (DOID:10983)
Alliance: disease page
Synonyms: Hereditary Nephritis
Alt IDs: MESH:D009394, ORDO:63, UMLS_CUI:C0027706
Definition: A syndrome disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss.

Disease References using Mouse Models (24)

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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