48,XXXY syndrome

Definition

Orphanet

The 48,XXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of two extra X chromosomes in males.

Go To Source: Orphanet

Other Classifiers and IDs

  • OrphaNet: ORPHA:96263
  • MedDRA: 10048228
  • UMLS: C0265498