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719657001: 2q23.1 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
3317267011 2q23.1 microdeletion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3317268018 2q23.1 microdeletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3317269014 Monosomy 2q23.1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3317270010 Pseudo-Angelman syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5402186011 The newly described 2q23.1 microdeletion syndrome includes severe intellectual deficit with pronounced speech delay, behavioral abnormalities including hyperactivity and inappropriate laughter, short stature and seizures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402187019 The newly described 2q23.1 microdeletion syndrome includes severe intellectual deficit with pronounced speech delay, behavioural abnormalities including hyperactivity and inappropriate laughter, short stature and seizures. 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
2q23.1 microdeletion syndrome (disorder) Is a Anomaly of chromosome pair 2 false Inferred relationship Some
2q23.1 microdeletion syndrome (disorder) Is a Deletion of part of autosome false Inferred relationship Some
2q23.1 microdeletion syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
2q23.1 microdeletion syndrome (disorder) Finding site Chromosome pair 2 false Inferred relationship Some 2
2q23.1 microdeletion syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
2q23.1 microdeletion syndrome (disorder) Finding site Chromosome pair 2 false Inferred relationship Some 3
2q23.1 microdeletion syndrome (disorder) Associated morphology Deletion of long arm false Inferred relationship Some 2
2q23.1 microdeletion syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) false Inferred relationship Some 3
2q23.1 microdeletion syndrome (disorder) Is a Deletion of part of long arm of chromosome 2 (disorder) true Inferred relationship Some
2q23.1 microdeletion syndrome (disorder) Finding site Chromosome pair 2 true Inferred relationship Some 1
2q23.1 microdeletion syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
2q23.1 microdeletion syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
2q23.1 microdeletion syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
2q23.1 microdeletion syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
2q23.1 microdeletion syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
2q23.1 microdeletion syndrome (disorder) Finding site Long arm of chromosome true Inferred relationship Some 2
2q23.1 microdeletion syndrome (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

GB English

US English

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