syndromic intellectual disability spastic paraplegia-nephritis-deafness syndrome Fitzsimmons Walson Mellor syndrome Fitzsimmons-Walson-Mellor syndrome GARD:0002342 MESH:C537937 MONDO:0008440 OMIM:182690 Orphanet:2820 This syndrome is characterised by variable spastic paraplegia, bilateral sensorineural deafness, intellectual deficit and progressive nephropathy. UMLS:C2931667 https://rarediseases.info.nih.gov/diseases/2342/fitzsimmons-walson-mellor-syndrome spastic paraplegia - nephritis - deafness spastic paraplegia, bilateral sensorineural deafness, intellectual retardation, and progressive nephropathy spastic paraplegia, sensorineural deafness, intellectual disability, and progressive nephropathy spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy autosomal dominant complex spastic paraplegia syndromic urogenital tract malformation syndromic genetic deafness syndromic renal or urinary tract malformation intellectual disability, autosomal dominant