RGD Annotation Report for Alport syndromeRat Genome Database

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An association has been curated linking MYH9 and Alport syndrome in Homo sapiens.

The association was inferred from experiment (EXP)
The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
25 RGD objects have been annotated to Alport syndrome (DOID:10983)
34 papers in RGD have been used to annotate MYH9
Curation Notes: CTD Direct Evidence: marker/mechanism
Original References(s): PMID:10973259

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.