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48,XXYY syndrome

Disease Summary
Associated Targets ()

Mondo Description The 48,XXYY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of an extra X and Y chromosome in males.
Mondo Term and Equivalent IDs
MONDO:0015028:  48,XXYY syndrome
GARD:0005677: 
NCIT:C89801: 
Orphanet:10: 
SCTID:403760006: 
UMLS:C2936741: