NLM Logo

Frasier Syndrome MeSH Descriptor Data 2024


MeSH Heading
Frasier Syndrome
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
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
2021/06/07
Frasier Syndrome Preferred
page delivered in 0.214s