U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Frasier Syndrome

A syndrome characterized by CHRONIC KIDNEY FAILURE and GONADAL DYSGENESIS in phenotypic females with karyotype of 46,XY or female individual with a normal 46,XX karyotype. It is caused by donor splice-site mutations of Wilms tumor suppressor gene (GENES, WILMS TUMOR) on chromosome 11.

Year introduced: 2006

PubMed search builder options

Subheadings:

Tree Number(s): C12.050.351.875.253.096.624, C12.050.351.968.419.780.750.500.500, C12.200.706.316.096.624, C12.200.777.419.780.750.500.500, C12.800.316.096.624, C12.950.419.780.750.500.500, C16.131.939.316.096.624, C16.320.306, C19.391.119.096.624, C23.550.291.500.906.500.500

MeSH Unique ID: D052159

Entry Terms:

  • Syndrome, Frasier

See Also:

Supplemental Content

Loading ...