Fragile X chromosome

Preferred Label : Fragile X chromosome;

Inclusion CIM-10 : Fragile X syndrome;

Diag associé à un acte (%) : 38.4;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q992;

UMLS CUI

C0432482;

Currated CISMeF NLP mapping
- Fragile X Syndrome [NCIt concept]
- Fragile X chromosome [ICD-10 Sub-category (who)]
- Fragile X chromosome [ICD-11 Category]
- Fragile X chromosome (disorder) [SNOMED CT concept]
- Fragile X syndrome [ORDO Disease]
- Fragile X syndrome [MedDRA Preferred Term]
- Fragile X syndrome [OMIM Phenotype]
- Fragile X syndrome [ICD-9 code]
- Fragile X syndrome (disorder) [SNOMED CT concept]
- fragile X syndrome [MeSH concept]
- fragile X syndrome [Disease (Nov.)]
- fragile X syndrome [DO Concept]
- fragile x syndrome [MeSH Descriptor]
- fragile x syndrome [MedlinePlus Topic]
- fragile x syndrome [SNOMED Notion]
- syndrome of the 'fragile x [medical devices type]
DO Cross reference
- fragile X syndrome [DO Concept]
Orphanet concepts
- Fragile X syndrome [ORDO Disease]
- Symptomatic form of fragile X syndrome in female carriers [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Fragile X chromosome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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