A condition caused by the presence of an extra X chromosome resulting in 47,XXX karyotype in an individual with female phenotype. The condition is characterized by tall stature, increased risk of learning disabilities, and delayed development of speech and language. [ NCI ]

Synonyms:

47,XXX Syndrome

47,XXX

Triple X Syndrome

Trisomy X

This is just here as a test because I lose it

Term information

Subsets

NCIT_C90259, NCIT_C165258, NCIT_C118467

ALT DEFINITION
  • A condition caused by the presence of an extra X chromosome resulting in 47,XXX karyotype in an individual with female phenotype. The condition is characterized by tall stature, increased risk of learning disabilities, and delayed development of speech and language.
Contributing Source
  • Cellosaurus
  • NICHD
Preferred Name
  • 47,XXX Syndrome
Semantic Type
  • Disease or Syndrome
UMLS CUI
  • C0221033
code
  • C129718

Term relations

Subclass of: