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48,XXYY syndrome

Disease Summary
Associated Targets (0)

Explore 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: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found