"Frasier Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D052159
|
| MeSH 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
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Frasier Syndrome".
- Diseases [C]
- Male Urogenital Diseases [C12]
- Urogenital Abnormalities [C12.706]
- Disorders of Sex Development [C12.706.316]
- 46, XY Disorders of Sex Development [C12.706.316.096]
- Frasier Syndrome [C12.706.316.096.624]
- Urologic Diseases [C12.777]
- Kidney Diseases [C12.777.419]
- Renal Insufficiency [C12.777.419.780]
- Renal Insufficiency, Chronic [C12.777.419.780.750]
- Kidney Failure, Chronic [C12.777.419.780.750.500]
- Frasier Syndrome [C12.777.419.780.750.500.500]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Female Urogenital Diseases [C13.351]
- Urogenital Abnormalities [C13.351.875]
- Disorders of Sex Development [C13.351.875.253]
- 46, XY Disorders of Sex Development [C13.351.875.253.096]
- Frasier Syndrome [C13.351.875.253.096.624]
- Urologic Diseases [C13.351.968]
- Kidney Diseases [C13.351.968.419]
- Renal Insufficiency [C13.351.968.419.780]
- Renal Insufficiency, Chronic [C13.351.968.419.780.750]
- Kidney Failure, Chronic [C13.351.968.419.780.750.500]
- Frasier Syndrome [C13.351.968.419.780.750.500.500]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
- Urogenital Abnormalities [C16.131.939]
- Disorders of Sex Development [C16.131.939.316]
- 46, XY Disorders of Sex Development [C16.131.939.316.096]
- Frasier Syndrome [C16.131.939.316.096.624]
- Genetic Diseases, Inborn [C16.320]
- Frasier Syndrome [C16.320.306]
- Endocrine System Diseases [C19]
- Gonadal Disorders [C19.391]
- Disorders of Sex Development [C19.391.119]
- 46, XY Disorders of Sex Development [C19.391.119.096]
- Frasier Syndrome [C19.391.119.096.624]
Below are MeSH descriptors whose meaning is more specific than "Frasier Syndrome".
This graph shows the total number of publications written about "Frasier Syndrome" by people in this website by year, and whether "Frasier Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 0 | 1 | 1 |
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Below are the most recent publications written about "Frasier Syndrome" by people in Profiles.
-
Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population. Physiol Genomics. 2005 Apr 14; 21(2):212-21.