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205672005: Chromosome inversion in normal individual (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
315417011 Chromosome inversion in normal individual en Synonym Active Entire term case insensitive SNOMED CT core module
591072014 Chromosome inversion in normal individual (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
Chromosome inversion in normal individual Is a Balanced rearrangement and structural marker true Inferred relationship Existential restriction modifier
Chromosome inversion in normal individual Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Chromosome inversion in normal individual Occurrence Congenital false Inferred relationship Existential restriction modifier
Chromosome inversion in normal individual Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Chromosome inversion in normal individual Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Chromosome inversion in normal individual Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Chromosome inversion in normal individual Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Chromosome inversion in normal individual 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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