has material basis in germline mutation in WT1 autosomal dominant disease syndromic disease Frasier syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/6753 https://rarediseases.info.nih.gov/diseases/2375/frasier-syndrome https://www.malacards.org/card/frasier_syndrome MONDO:0007635 Frasier syndrome, autosomal dominant, somatic mutation UMLS:C0950122 SCTID:445431000 MESH:D052159 Frasier syndrome is characterized by the association of male pseudohermaphrodism and glomerular nephropathy. This syndrome is associated with a high risk of developing gonadoblastoma. DOID:0050438 Orphanet:347 GARD:0002375 Frasier syndrome icd11.foundation:1659542949 NCIT:C122805 ICD9:759.89 OMIM:136680 MEDGEN:215533 46 XY differences of sex development