disease has basis in dysfunction of WT1 autosomal dominant disease syndromic disease Frasier syndrome DOID:0050438 Frasier syndrome Frasier syndrome is characterised by the association of male pseudohermaphrodism and glomerular nephropathy. This syndrome is associated with a high risk of developing gonadoblastoma. GARD:0002375 ICD10:N04.1 ICD9:759.89 MESH:D052159 MONDO:0007635 NCIT:C122805 OMIM:136680 Orphanet:347 SCTID:445431000 UMLS:C0950122 https://rarediseases.info.nih.gov/diseases/2375/frasier-syndrome primary glomerular disease polymalformative genetic syndrome with increased risk of developing cancer syndrome with 46,XY disorder of sex development