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syndromic diseae characterized by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss. [Orphanet:886]","descendants":["MONDO:0010168","MONDO:0012968","MONDO:0010775","MONDO:0014001","MONDO:0700087","MONDO:0010170","MONDO:0029141","MONDO:0011186","MONDO:0010171","MONDO:0011558","MONDO:0010984","MONDO:0011195","MONDO:0010169","MONDO:0013788","MONDO:0016484","MONDO:0012662","MONDO:0016485","MONDO:0011748","MONDO:0100050"],"label":"Usher syndrome","mondo":"MONDO:0019501","parents":["MONDO:0002254","MONDO:0006025"],"should_conform_to":{"http":["http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml"]},"synonym":{"exact":["USH","ush","Usher's syndrome"],"related":["dystrophia retinae pigmentosa-dysostosis syndrome","Graefe-Usher syndrome","Hallgren syndrome"]},"xrefs":{"doid":["DOID:0050439"],"gard":["0007843"],"icd11":["foundation:1452641873"],"meddra":["10063396"],"mesh":["D052245"],"nando":["1200941"],"ncit":["C85217"],"nord":["1816"],"omimps":["276900"],"orphanet":["886"]}},"original_id":"orphanet:886"}