Medical entity reference · Cardiology
Turner syndrome
Wikidata · Retrieved 2026-10-13
Chromosomal variation where a person is born with a 45X chromosome pattern rather than the typical 46XX. Wikidata entity Q202849; linked MeSH descriptor D014424. Includes multilingual names and external identifier mappings.
Reference details
- Wikidata entity
- Q202849
- Revision
- 2555939067
- MeSH
- D014424
- Disease Ontology
- DOID:3491
- UMLS
- C0041408; C1527168
- ICD-10
- Q96
Entity description
chromosomal variation where a person is born with a 45X chromosome pattern rather than the typical 46XX
Names in different languages
en: Turner syndrome
zh: 特纳氏综合症
zh-hans: 特纳氏综合症
ja: ターナー症候群
es: síndrome de Turner
fr: syndrome de Turner
de: Turner-Syndrom
pt: síndrome de Turner
ar: متلازمة تيرنر
ru: Синдром Шерешевского — Тёрнера
English alternative names
Bonnevie-Ullrich syndrome
Bonnevie-Ullrich syndrome NOS
Bonnevie-Ullrich syndrome NOS (disorder)
Gonadal dysgenesis - Turner
Karyotype 45, X
Monosomy X
Turner syndrome (disorder)
Turner's syndrome NOS
Turner's syndrome NOS (disorder)
XO syndrome
monosomy X syndrome
Ullrich–Turner syndrome
Turner's syndrome
Identifier mapping
MeSH: D014424
Disease Ontology: DOID:3491
UMLS: C0041408; C1527168
ICD-10: Q96
Sources and reuse
Structured entity record with names and identifiers. Check individual statements and references at the source.
Source date: 2026-10-11T17:45:07Z. Retrieved: 2026-10-13. Text has been organized for reading; this import has not been independently reviewed by a clinician. It is not individualized medical advice.