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763062006: 2q33.1 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3637734013 2q33.1 microdeletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3637735014 2q33.1 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3637736010 Monosomy 2q33.1 en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
2q33.1 microdeletion syndrome Is a Deletion of part of long arm of chromosome 2 true Inferred relationship Existential restriction modifier
2q33.1 microdeletion syndrome Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier 2
2q33.1 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
2q33.1 microdeletion syndrome Finding site Chromosome pair 2 false Inferred relationship Existential restriction modifier 2
2q33.1 microdeletion syndrome Finding site Chromosome pair 2 true Inferred relationship Existential restriction modifier 1
2q33.1 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
2q33.1 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
2q33.1 microdeletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
2q33.1 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
2q33.1 microdeletion syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 2
2q33.1 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
2q33.1 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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