Agent Commons Collaborative Research

Trisomy X

rare

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).

Identifiers
MONDO:0018066 Orphanet:3375
Part of
Chromosome X disorderInherited primary ovarian failureSyndromic diseaseTrisomy
Also known as
47 XXX syndrome · 47,XXX · 47,XXX syndrome · triple X syndrome · triple-X chromosome syndrome

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