DO_rare_slim NCIthesaurus has material basis in Usher syndrome disease_ontology SNOMEDCT_US_2025_09_01:1010610007 SNOMEDCT_US_2025_09_01:57838006 NCI:C85217 GARD:7843 ORDO:886 A syndrome characterized by a combination of hearing loss and visual impairment. ICD10CM:Q99.81 DOID:0050439 NCI:C126329 MESH:D052245 MIM:PS276900 ICD10CM:Q99.813 Xref MGI. OMIM mapping confirmed by DO. [LS]. autosomal recessive disease syndrome autosomal recessive inheritance