klinefelter syndrome

Preferred Label : klinefelter syndrome;

Details

Origin ID

D4-02252;

UMLS CUI

C0022735;

Automatic exact mappings (from CISMeF team)
- XXY trisomy [MeSH concept]
- congenital anomaly nos/multiple [ICPC-2 Rubric]
- klinefelter syndrome [EMDN type]
Currated CISMeF NLP mapping
- KLINEFELTER'S SYNDROME [WHO-ART Included Term]
- Klinefelter Syndrome [NCIt concept]
- Klinefelter syndrome [PASCAL descriptor]
- Klinefelter syndrome [DO Concept]
- Klinefelter syndrome [Disease (Nov.)]
- Klinefelter syndrome [ICD-11 Subcategory]
- Klinefelter syndrome [ORDO Disease]
- Klinefelter syndrome (disorder) [SNOMED CT concept]
- Klinefelter syndrome, unspecified [ICD-10 Sub-category]
- Klinefelter's syndrome [ICD-9 code]
- Klinefelter's syndrome [MedDRA Preferred Term]
- Klinefelter's syndrome - male with more than two X chromosomes (disorder) [Inactive SNOMED CT concept]
- Klinefelter's syndrome, XXY (disorder) [SNOMED CT concept]
- Klinefelters syndrome, unspecified [ICD-10 Sub-category (who)]
- XXY syndrome [MedDRA LLT]
- klinefelter syndrome [MeSH Descriptor]
- klinefelter syndrome [MeSH concept]
- klinefelter syndrome [medical devices type]
- klinefelter's syndrome [MedlinePlus Topic]
ICD-10 exact mapping(s)
- Klinefelters syndrome karyotype 47,XXY [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- 48,XXXY syndrome [ORDO Disease]
- 49,XXXXY syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Male infertility due to gonadal dysgenesis [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
See also inter- (CISMeF)
- hypogonadotropic hypogonadism [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- KLINEFELTER'S SYNDROME [WHO-ART Included Term]
- Klinefelter Syndrome [NCIt concept]
- Klinefelter syndrome [ORDO Disease]
- Klinefelter syndrome [Disease (Nov.)]
- Klinefelter syndrome [DO Concept]
- Klinefelter syndrome [PASCAL descriptor]
- Klinefelter syndrome [ACR pathology]
- Klinefelter syndrome [ICD-11 Subcategory]
- Klinefelter syndrome (disorder) [SNOMED CT concept]
- Klinefelter syndrome karyotype 47, XXY [ICD-10 Sub-category]
- Klinefelter syndrome, unspecified [ICD-10 Sub-category]
- Klinefelter's syndrome [ICD-9 code]
- Klinefelter's syndrome [MedDRA Preferred Term]
- Klinefelter's syndrome, XXY (disorder) [SNOMED CT concept]
- Klinefelters syndrome, unspecified [ICD-10 Sub-category (who)]
- XXY syndrome [MedDRA LLT]
- klinefelter syndrome [MeSH concept]
- klinefelter syndrome [MeSH Descriptor]
- klinefelter's syndrome [MedlinePlus Topic]
Validated automatic mappings to BTNT
- Klinefelter syndrome with karyotype 47,XXY, regular [ICD-11 Sub-sub category]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients