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254261005: Pseudotrisomy 18 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
378491010 Pseudotrisomy 18 en Synonym Active Entire term case insensitive SNOMED CT core module
645129013 Pseudotrisomy 18 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pseudotrisomy 18 Is a Congenital disorder due to abnormality of chromosome number OR structure true Inferred relationship Existential restriction modifier
Pseudotrisomy 18 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Pseudotrisomy 18 Occurrence Congenital false Inferred relationship Existential restriction modifier
Pseudotrisomy 18 Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Pseudotrisomy 18 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Pseudotrisomy 18 Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Pseudotrisomy 18 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Pseudotrisomy 18 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Pseudotrisomy 18 Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Pseudotrisomy 18 Finding site Chromosome structure 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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