719018008: déficience intellectuelle liée à l'X type Abidi (trouble)

• SNOMED CT Concept\constatation clinique\Disease\...
• \Genetic disease\maladie héréditaire\...
• \Developmental hereditary disorder\X-linked intellectual disability Abidi type (disorder)
• \Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\X-linked intellectual disability Abidi type (disorder)
• \trouble mental\troubles mentaux du développement\Intellectual disability\X-linked intellectual disability Abidi type (disorder)
• \Congenital disease\Congenital malformation\Congenital malformation syndrome (disorder)\X-linked intellectual disability Abidi type (disorder)
• \trouble du développement\Neurodevelopmental disorder\troubles mentaux du développement\Intellectual disability\X-linked intellectual disability Abidi type (disorder)
• \trouble du développement\Developmental hereditary disorder\X-linked intellectual disability Abidi type (disorder)
• \trouble du développement\Congenital malformation\Congenital malformation syndrome (disorder)\X-linked intellectual disability Abidi type (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3314685019	X-linked intellectual disability Abidi type (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3314686018	X-linked intellectual disability Abidi type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
753451000241111	déficience intellectuelle liée à l'X type Abidi (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
983161000172110	déficience intellectuelle liée à l'X type Abidi	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3314687010	This syndrome has characteristics of X-linked intellectual deficit and mild variable manifestations, including short stature, small head circumference, sloping forehead, hearing loss, abnormally shaped ears, and small testes. It has been described in eight affected males from three generations.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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