turner syndrome, nos

Preferred Label : turner syndrome, nos;

Details

Origin ID

D4-02272;

UMLS CUI

C0041408;

Automatic exact mappings (from CISMeF team)
- Bonnevie-Ullrich Syndrome [NCIt concept]
- Bonnevie-Ullrich syndrome [MedDRA LLT]
- Bonnevie-Ullrich syndrome [MeSH concept]
- congenital anomaly nos/multiple [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Karyotype 45, X [ICD-10 Sub-category]
- 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 [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 [ORDO Disease]
- Turner syndrome (disorder) [SNOMED CT concept]
- Turner's syndrome [ICD-10 category]
- Turner's syndrome [MedDRA Preferred Term]
- Turner's syndrome, unspecified [ICD-10 Sub-category]
- Turners syndrome [ICD-10 category (who)]
- Turners syndrome, unspecified [ICD-10 Sub-category (who)]
- XO Syndrome [NCIt concept]
- XO genotype [MedDRA LLT]
- gonadal dysgenesis syndrome [Radlex concept]
- turner syndrome [MeSH Descriptor]
- turner syndrome [MeSH concept]
- turner syndrome [MedlinePlus Topic]
False automatic mappings
- noonan syndrome [MeSH Descriptor]
ICD-10 exact mapping(s)
- Turners syndrome, unspecified [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Monosomy X [ORDO Disease]
- Mosaic monosomy X [ORDO Disease]
- Turner syndrome due to structural X chromosome anomalies [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Chromosomal anomaly with cataract [ORDO Disease]
- Gonadal dysgenesis of gynecological interest [ORDO Disease]
- Non-acquired premature ovarian failure [ORDO Disease]
- Rare endocrine growth disease [ORDO Disease]
- Rare female infertility [ORDO Disease]
- Sex-chromosome number anomaly [ORDO Disease]
- Syndromic developmental defect of the eye [ORDO Disease]
- Syndromic epicanthus [ORDO Disease]
- Syndromic renal or urinary tract malformation [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Turner syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Karyotype 45, X [ICD-10 Sub-category]
- 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 [ICD-10 category]
- Turner's syndrome [MedDRA Preferred Term]
- Turner's syndrome, unspecified [ICD-10 Sub-category]
- 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 Descriptor]
- turner syndrome [MeSH concept]
- turner syndrome [MedlinePlus Topic]
Validated automatic mappings to BTNT
- Karyotype 45, X [ICD-11 Sub-sub category]

Keyword's position in hierarchy(ies) :

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