trisomy X (Q10185): Difference between revisions

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(‎Created claim: GSSO V2 ID (P25): 007097)
(‎Created claim: Homosaurus Version 3 ID (P26): homoit0002878)
Property / Homosaurus Version 3 ID
 
Property / Homosaurus Version 3 ID: homoit0002878 / rank
 
Normal rank

Revision as of 17:13, 9 October 2023

A human chromosomal copy number variation consisting of the presence of a third copy of the X chromosome in somatic cells, making the person's karyotype 47,XXX.
  • trisomy of the X chromosome
  • trisomy of chromosome X
  • X trisomy
Language Label Description Also known as
English
trisomy X
A human chromosomal copy number variation consisting of the presence of a third copy of the X chromosome in somatic cells, making the person's karyotype 47,XXX.
  • trisomy of the X chromosome
  • trisomy of chromosome X
  • X trisomy

Statements