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717049005: Trisomy 17p (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
3308283018 Trisomy 17p (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3308284012 Trisomy 17p 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
Trisomy 17p Is a 17p partial trisomy syndrome true Inferred relationship Existential restriction modifier
Trisomy 17p Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Trisomy 17p Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Trisomy 17p Finding site Face structure true Inferred relationship Existential restriction modifier 2
Trisomy 17p Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Trisomy 17p Associated morphology Partial trisomy false Inferred relationship Existential restriction modifier 2
Trisomy 17p Finding site Chromosome pair 17 false Inferred relationship Existential restriction modifier 2
Trisomy 17p Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Trisomy 17p Finding site Face structure false Inferred relationship Existential restriction modifier 3
Trisomy 17p Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Trisomy 17p Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Trisomy 17p Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Trisomy 17p Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Trisomy 17p Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
Trisomy 17p Finding site Chromosome pair 17 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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