 Frasier Syndrome
"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
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| 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
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| Concept/Terms |
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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".
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Below are the most recent publications written about "Frasier Syndrome" by people in Profiles.
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