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trisomy X

Disease Summary
Associated Targets (0)

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Mondo Description Trisomy X is a sex chromosome anomaly with a variable phenotype caused by the presence of an extra X chromosome in females (47,XXX instead of 46,XX).
Mondo Term and Equivalent IDs
MONDO:0018066:  trisomy X
GARD:0005672: 
MESH:C535318: 
NCIT:C129718: 
Orphanet:3375: 
SCTID:35111009: 
UMLS:C0221033: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found