 Sex Chromosome Disorders
"Sex Chromosome Disorders" 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.
Clinical conditions caused by an abnormal sex chromosome constitution (SEX CHROMOSOME ABERRATIONS), in which there is extra or missing sex chromosome material (either a whole chromosome or a chromosome segment).
| Descriptor ID |
D025064
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| MeSH Number(s) |
C16.131.260.830 C16.320.180.830
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| Concept/Terms |
Sex Chromosome Disorders- Sex Chromosome Disorders
- Disorders, Sex Chromosome Abnormality
- Sex Chromosome Abnormality Disorders
- Disorders, Sex Chromosome
- Chromosome Disorder, Sex
- Chromosome Disorders, Sex
- Sex Chromosome Disorder
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Below are MeSH descriptors whose meaning is more general than "Sex Chromosome Disorders".
Below are MeSH descriptors whose meaning is more specific than "Sex Chromosome Disorders".
This graph shows the total number of publications written about "Sex Chromosome Disorders" by people in this website by year, and whether "Sex Chromosome Disorders" 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 |
|---|
| 2004 | 0 | 1 | 1 | | 2015 | 2 | 0 | 2 |
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Below are the most recent publications written about "Sex Chromosome Disorders" by people in Profiles.
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Grams SE, Argiropoulos B, Lines M, Chakraborty P, Mcgowan-Jordan J, Geraghty MT, Tsang M, Eswara M, Tezcan K, Adams KL, Linck L, Himes P, Kostiner D, Zand DJ, Stalker H, Driscoll DJ, Huang T, Rosenfeld JA, Li X, Chen E. Genotype-phenotype characterization in 13 individuals with chromosome Xp11.22 duplications. Am J Med Genet A. 2016 Apr; 170A(4):967-77.
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Samango-Sprouse C, Stapleton EJ, Lawson P, Mitchell F, Sadeghin T, Powell S, Gropman AL. Positive effects of early androgen therapy on the behavioral phenotype of boys with 47,XXY. Am J Med Genet C Semin Med Genet. 2015 Jun; 169(2):150-7.
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Kato M, Das S, Petras K, Kitamura K, Morohashi K, Abuelo DN, Barr M, Bonneau D, Brady AF, Carpenter NJ, Cipero KL, Frisone F, Fukuda T, Guerrini R, Iida E, Itoh M, Lewanda AF, Nanba Y, Oka A, Proud VK, Saugier-Veber P, Schelley SL, Selicorni A, Shaner R, Silengo M, Stewart F, Sugiyama N, Toyama J, Toutain A, Vargas AL, Yanazawa M, Zackai EH, Dobyns WB. Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation. Hum Mutat. 2004 Feb; 23(2):147-59.
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