Fragile X chromosome

ICD-11 code : LD55;

Preferred Label : Fragile X chromosome;

ICD-11 definition : Fragile X syndrome is a rare genetic disease associated with mild to severe intellectual deficit that may be associated with behavioral disorders and characteristic physical features.;

ICD-11 inclusion : fraxa - fragile x syndrome; marker x syndrome; Fragile X syndrome; martin-bell syndrome;

Details

Origin ID

1524287677;

Currated CISMeF NLP mapping
- Fragile X Syndrome [NCIt concept]
- Fragile X chromosome [ICD-10 Sub-category]
- Fragile X chromosome [ICD-10 Sub-category (who)]
- 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 [Disease (Nov.)]
- fragile X syndrome [DO Concept]
- fragile X syndrome [MeSH concept]
- fragile x syndrome [MeSH Descriptor]
- fragile x syndrome [MedlinePlus Topic]
- fragile x syndrome [SNOMED Notion]
- syndrome of the 'fragile x [medical devices type]
ICD-10 Mapping
- Fragile X chromosome [ICD-10 Sub-category]

Keyword's position in hierarchy(ies) :

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