Turner's syndrome

Preferred Label : Turner's syndrome;

ICD-10 exclusion note : Noonan syndrome (Q87.1);

Rare : true;

Source : OMS;

Date de début : 01/01/1997;

Do not code with : true;

Details

Origin ID

Q96;

UMLS CUI

C0041408;

Automatic exact mappings (from CISMeF team)
- congenital anomaly nos/multiple [ICPC-2 Rubric]
- turner syndrome [EMDN type]
Currated CISMeF NLP mapping
- Karyotype 45,X [ICD-10 Sub-category (who)]
- Monosomy X [NCIt concept]
- Monosomy X [ORDO Disease]
- Monosomy X (disorder) [SNOMED CT concept]
- TURNER'S SYNDROME [WHO-ART Included Term]
- Turner Syndrome [NCIt concept]
- Turner syndrome [ORDO Disease]
- Turner syndrome [PASCAL descriptor]
- Turner syndrome [Disease (Nov.)]
- Turner syndrome [DO Concept]
- Turner syndrome [ACR pathology]
- Turner syndrome [ACR pathology]
- Turner syndrome [ICD-11 Subcategory]
- Turner syndrome (disorder) [SNOMED CT concept]
- Turner's syndrome [MedDRA Preferred Term]
- Turners syndrome [ICD-10 category (who)]
- Turners syndrome, unspecified [ICD-10 Sub-category (who)]
- XO Syndrome [NCIt concept]
- XO genotype [MedDRA LLT]
- turner syndrome [MeSH concept]
- turner syndrome [MeSH Descriptor]
- turner syndrome [MedlinePlus Topic]
- turner syndrome, nos [SNOMED Notion]
DO Cross reference
- Turner syndrome [DO Concept]
Excluded by
- Congenital absence of ovary [ICD-10 Sub-category]
- Indeterminate sex and pseudohermaphroditism [ICD-10 category]
- Other sex chromosome abnormalities, female phenotype, not elsewhere classified [ICD-10 category]
- Primary ovarian failure [ICD-10 Sub-category]
ICD-10 exclusion(s)
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category]
Manual NTBT mappings (CISMeF)
- Monosomy X [ORDO Disease]
- Mosaic monosomy X [ORDO Disease]
- Turner syndrome due to structural X chromosome anomalies [ORDO Disease]
Metaterm(s)
- genetics [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Karyotype 45, X [ICD-11 Sub-sub category]
- Monosomy X [ORDO Disease]
- TURNER'S SYNDROME [WHO-ART Included Term]
- Turner Syndrome [NCIt concept]
- Turner syndrome [PASCAL descriptor]
- Turner syndrome [ACR pathology]
- Turner syndrome [ACR pathology]
- Turner syndrome [ACR pathology]
- Turner syndrome (disorder) [SNOMED CT concept]
- Turner's syndrome [MedDRA Preferred Term]
- XO Syndrome [NCIt concept]
- XO genotype [MedDRA LLT]
- turner syndrome [MeSH Descriptor]
- turner syndrome [MedlinePlus Topic]
- turner syndrome [MeSH concept]
- turner syndrome, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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