"Gonadoblastoma" 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 complex neoplasm composed of a mixture of gonadal elements, such as large primordial GERM CELLS, immature SERTOLI CELLS or GRANULOSA CELLS of the sex cord, and gonadal stromal cells. Gonadoblastomas are most often associated with gonadal dysgenesis, 46, XY.
| Descriptor ID |
D018238
|
| MeSH Number(s) |
C04.557.465.420 C04.557.475.395 C12.706.316.096.687.500 C12.706.316.309.388.500 C13.351.875.253.096.687.500 C13.351.875.253.309.388.500 C16.131.939.316.096.687.500 C16.131.939.316.309.388.500 C19.391.119.096.687.500 C19.391.119.309.388.500
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Gonadoblastoma".
- Diseases [C]
- Neoplasms [C04]
- Neoplasms by Histologic Type [C04.557]
- Neoplasms, Germ Cell and Embryonal [C04.557.465]
- Gonadoblastoma [C04.557.465.420]
- Neoplasms, Gonadal Tissue [C04.557.475]
- Gonadoblastoma [C04.557.475.395]
- 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]
- Gonadal Dysgenesis, 46,XY [C12.706.316.096.687]
- Gonadoblastoma [C12.706.316.096.687.500]
- Gonadal Dysgenesis [C12.706.316.309]
- Gonadal Dysgenesis, 46,XY [C12.706.316.309.388]
- Gonadoblastoma [C12.706.316.309.388.500]
- 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]
- Gonadal Dysgenesis, 46,XY [C13.351.875.253.096.687]
- Gonadoblastoma [C13.351.875.253.096.687.500]
- Gonadal Dysgenesis [C13.351.875.253.309]
- Gonadal Dysgenesis, 46,XY [C13.351.875.253.309.388]
- Gonadoblastoma [C13.351.875.253.309.388.500]
- 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]
- Gonadal Dysgenesis, 46,XY [C16.131.939.316.096.687]
- Gonadoblastoma [C16.131.939.316.096.687.500]
- Gonadal Dysgenesis [C16.131.939.316.309]
- Gonadal Dysgenesis, 46,XY [C16.131.939.316.309.388]
- Gonadoblastoma [C16.131.939.316.309.388.500]
- 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]
- Gonadal Dysgenesis, 46,XY [C19.391.119.096.687]
- Gonadoblastoma [C19.391.119.096.687.500]
- Gonadal Dysgenesis [C19.391.119.309]
- Gonadal Dysgenesis, 46,XY [C19.391.119.309.388]
- Gonadoblastoma [C19.391.119.309.388.500]
Below are MeSH descriptors whose meaning is more specific than "Gonadoblastoma".
This graph shows the total number of publications written about "Gonadoblastoma" by people in this website by year, and whether "Gonadoblastoma" 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 |
|---|
| 2000 | 0 | 1 | 1 |
| 2009 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Gonadoblastoma" by people in Profiles.
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Bilateral gonadoblastoma with dysgerminoma and pilocytic astrocytoma with WT1 GT-IVS9 mutation: A 46 XY phenotypic female with Frasier syndrome. Pediatr Blood Cancer. 2009 Dec 15; 53(7):1349-51.
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Identification of Y chromatin directly in gonadal tissue by fluorescence in situ hybridization (FISH): significance for Ullrich-Turner syndrome screening in the cytogenetics laboratory. Am J Med Genet. 2000 Apr 24; 91(5):377-82.