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699308002: Microdeletion of chromosome 15q24 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2983610010 15q24 microdeletion en Synonym Active Entire term case insensitive SNOMED CT core module
2983637012 15q24 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2983648017 Interstitial deletion of chromosome 15q24 en Synonym Active Entire term case insensitive SNOMED CT core module
2983696017 Microdeletion of chromosome 15q24 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2983720014 15q24 deletion en Synonym Active Entire term case insensitive SNOMED CT core module
3023268018 Microdeletion of chromosome 15q24 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
Microdeletion of chromosome 15q24 Is a Anomaly of chromosome pair 15 false Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q24 Occurrence Congenital false Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q24 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q24 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q24 Finding site Chromosome pair 15 false Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q24 Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q24 Is a Partial deletion of long arm of chromosome 15 true Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q24 Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q24 Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q24 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q24 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Microdeletion of chromosome 15q24 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Microdeletion of chromosome 15q24 Finding site Chromosome pair 15 true Inferred relationship Existential restriction modifier 2
Microdeletion of chromosome 15q24 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
Microdeletion of chromosome 15q24 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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