RHYNS syndrome GARD:0009681 MESH:C537612 MONDO:0011202 OMIM:602152 Orphanet:140976 RHYNS syndrome RHYNS syndrome is characterised by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia. SCTID:723999009 UMLS:C1865794 retinitis pigmentosa syndrome retinitis pigmentosa, hypopituitarism, nephronophthisis, and mild skeletal dysplasia retinitis pigmentosa-hypopituitarism-nephronophthisis-skeletal dysplasia syndrome inherited renal tubular disease rare renal tubular disease syndromic retinitis pigmentosa