719599008: syndrome de microdélétion 19q13.11 (trouble)

• SNOMED CT Concept\constatation clinique\Disease\...
• \anomalie chromosomique\maladie chromosomique congénitale\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 19 (disorder)\Deletion of long arm of chromosome 19 (disorder)\19q13.11 microdeletion syndrome (disorder)
• \Anomaly of chromosome pair 19\Deletion of part of chromosome 19 (disorder)\Deletion of long arm of chromosome 19 (disorder)\19q13.11 microdeletion syndrome (disorder)
• \trouble mental\troubles mentaux du développement\Intellectual disability\19q13.11 microdeletion syndrome (disorder)
• \Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 19 (disorder)\Deletion of long arm of chromosome 19 (disorder)\19q13.11 microdeletion syndrome (disorder)
• \Anomaly of chromosome pair 19\Deletion of part of chromosome 19 (disorder)\Deletion of long arm of chromosome 19 (disorder)\19q13.11 microdeletion syndrome (disorder)
• \trouble du développement\Neurodevelopmental disorder\troubles mentaux du développement\Intellectual disability\19q13.11 microdeletion syndrome (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
3317092018	19q13.11 microdeletion syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3317093011	19q13.11 microdeletion syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3317094017	Monosomy 19q13.11	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
754531000241117	syndrome de microdélétion 19q13.11 (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
870201000172113	del(19)(q13.11)	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
946361000172111	syndrome de microdélétion 19q13.11	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3317095016	The 19q13.11 microdeletion has characteristics of several major features including pre and postnatal growth retardation, slender habitus, severe postnatal feeding difficulties, microcephaly, intellectual deficit with speech disturbance, hypospadias and ectodermal dysplasia presented by scalp aplasia, thin and sparse hair, eyebrows and eyelashes, thin and dry skin and dysplastic nails. To date, the syndrome has been identified in five patients. Haploinsufficiency of one or more genes in the 19q13.11 region could cause this microdeletion syndrome.	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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