FG syndrome - CISMeF

Preferred Label : FG syndrome;

ICD-11 definition : FG syndrome (FGS) is aX-linked recessive multiple congenital anomalies (MCA) and developmental delay syndrome with a characteristic psychological pattern (delayed development of sensory integration, attention deficit disorder, self-absorption and fascinations with mechanical toys and objects). Males are affected, but carrier girls and women may also be affected, sometimes more severely than the males.;

ICD-11 synonym : Keller syndrome; Opitz-Kaveggia syndrome;

Détails

Origin ID

156523187;

Currated CISMeF NLP mapping
- FG syndrome [DO Concept]
- FG syndrome [ORDO Disease]
- FG syndrome [Disease (Nov.)]
- FG syndrome (disorder) [SNOMED CT concept]
- Fg syndrome [OMIM phenotypic series]
- Opitz-Kaveggia syndrome [MeSH Supplementary Concept]
- Opitz-Kaveggia syndrome [MeSH concept]
- Opitz-kaveggia syndrome [OMIM Phenotype]
- fg syndrome [SNOMED Notion]
Validated automatic mappings to BTNT
- FG Syndrome Type 1 [NCIt concept]
- FG syndrome type 1 [ORDO Disease]

Position du mot-clé dans l'(les) arborescence(s) :

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