LD51ICD-11 MMS 2026-01
Structural anomalies of chromosome X, excluding Turner syndrome
Index terms
- Structural anomalies of chromosome X, excluding Turner syndrome
- Small ring X chromosome
- Xp11.22p11.23 duplication
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- Trisomy Xp11.22p11.23
- Xp11.22p11.23 duplication syndrome
- Xp11.3 deletion
- Xp21 deletion
- Xp21 deletion syndrome
- Xp22.13p22.2 duplication
- Xp22.33 deletion
- Xq27.3q28 duplication
- Xq28 deletion
- Distal monosomy Xq
- Xq28 deletion syndrome
- Xq28 duplication
- Distal duplication Xq
- Telomeric duplication Xq
- Xq28 duplication syndrome
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LD50– Number anomalies of chromosome XLD52– Number anomalies of chromosome YLD53– Structural anomalies of chromosome YLD54– Male with sex chromosome mosaicismLD55– Fragile X chromosomeLD56– Chimaera 46, XX, 46, XYLD5Y– Other specified sex chromosome anomaliesLD5Z– Sex chromosome anomalies, unspecified
Foundation entity
Structural anomalies of chromosome X, excluding Turner syndrome – http://id.who.int/icd/entity/2055488559
Part of: 20: Developmental anomalies