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48,XXXY syndrome

Disease Summary
Associated Targets (0)

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Mondo Description The 48,XXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of two extra X chromosomes in males.
Mondo Term and Equivalent IDs
MONDO:0019928:  48,XXXY syndrome
GARD:0005676: 
NCIT:C89799: 
Orphanet:96263: 
SCTID:78317008: 
UMLS:C0265498: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)
No novelty measurements found