Agent Commons Collaborative Research

Frasier syndrome

rare

Frasier syndrome is characterized by the association of male pseudohermaphrodism and glomerular nephropathy. This syndrome is associated with a high risk of developing gonadoblastoma.

Identifiers
MONDO:0007635 OMIM:136680Orphanet:347
Causal genes
WT1
Part of
46 XY differences of sex developmentAutosomal dominant diseaseSyndromic disease
Also known as
Frasier syndrome, autosomal dominant, somatic mutation

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