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716515000: 1q41q42 microdeletion syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3306159010 1q41q42 microdeletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3306160017 1q41q42 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3306161018 Monosomy 1q41q42 en Synonym Active Entire term case insensitive SNOMED CT core module
3306162013 1q41-q42 microdeletion syndrome 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
1q41q42 microdeletion syndrome Is a Anomaly of chromosome pair 1 false Inferred relationship Existential restriction modifier
1q41q42 microdeletion syndrome Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier
1q41q42 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
1q41q42 microdeletion syndrome Finding site Chromosome pair 1 true Inferred relationship Existential restriction modifier 2
1q41q42 microdeletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
1q41q42 microdeletion syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 3
1q41q42 microdeletion syndrome Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier 2
1q41q42 microdeletion syndrome Associated morphology Partial monosomy false Inferred relationship Existential restriction modifier 3
1q41q42 microdeletion syndrome Is a 1q partial monosomy true Inferred relationship Existential restriction modifier
1q41q42 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
1q41q42 microdeletion syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 1
1q41q42 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
1q41q42 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
1q41q42 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
1q41q42 microdeletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
1q41q42 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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