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716381003: syndrome de microdélétion 8p23.1 (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3305744017 8p23.1 microdeletion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3305745016 8p23.1 microdeletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3305746015 Monosomy 8p23.1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
749661000241112 syndrome de microdélétion 8p23.1 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
951191000172110 del(8)(p23.1) fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
996161000172118 syndrome de microdélétion 8p23.1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3305747012 A partial deletion of the short arm of chromosome 8 with manifestations of low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects. The prevalence is unknown but 8p23.1 deletions are rare. The clinical manifestations are variable and do not depend on the size of the deletion, since this is the same in the majority of patients. Most 8p23.1 deletions occur de novo, however, parents can carry and transmit the chromosomal rearrangement to their children as well, with a risk of 50% for each child. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
8p23.1 microdeletion syndrome (disorder) est un(e) (attribut) 8p partial monosomy syndrome true Inferred relationship Some
8p23.1 microdeletion syndrome (disorder) morphologie associée (attribut) Deletion of short arm true Inferred relationship Some 2
8p23.1 microdeletion syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 2
8p23.1 microdeletion syndrome (disorder) localisation d'une constatation (attribut) Chromosome pair 8 (cell structure) true Inferred relationship Some 2
8p23.1 microdeletion syndrome (disorder) morphologie associée (attribut) Partial monosomy (morphologic abnormality) true Inferred relationship Some 3
8p23.1 microdeletion syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 3
8p23.1 microdeletion syndrome (disorder) localisation d'une constatation (attribut) Chromosome pair 8 (cell structure) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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