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Frasier Syndrome MeSH Descriptor Data 2021


MeSH Heading
Frasier Syndrome
Tree Number(s)
C12.706.316.096.624
C12.777.419.780.750.500.500
C13.351.875.253.096.624
C13.351.968.419.780.750.500.500
C16.131.939.316.096.624
C16.320.306
C19.391.119.096.624
Unique ID
D052159
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D052159
Annotation
do not confuse with FRASER SYNDROME
Scope Note
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.
See Also
Fraser Syndrome
Public MeSH Note
2006; see DENYS-DRASH SYNDROME 2002-2005
History Note
2006; use DENYS-DRASH SYNDROME 2002-2005
Date Established
2006/01/01
Date of Entry
2005/06/30
Revision Date
2012/07/03
Frasier Syndrome Preferred
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