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726733007: Chromosome Xp22.3 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3452288011 Chromosome Xp22.3 microdeletion syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3452289015 Chromosome Xp22.3 microdeletion syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3452290012 Xp22.3 microdeletion syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosome Xp22.3 microdeletion syndrome Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier
Chromosome Xp22.3 microdeletion syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Chromosome Xp22.3 microdeletion syndrome Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier
Chromosome Xp22.3 microdeletion syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 2
Chromosome Xp22.3 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Chromosome Xp22.3 microdeletion syndrome Finding site Sex chromosome X true Inferred relationship Existential restriction modifier 2
Chromosome Xp22.3 microdeletion syndrome Associated morphology Partial monosomy false Inferred relationship Existential restriction modifier 3
Chromosome Xp22.3 microdeletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Chromosome Xp22.3 microdeletion syndrome Finding site Sex chromosome X false Inferred relationship Existential restriction modifier 3
Chromosome Xp22.3 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Chromosome Xp22.3 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Chromosome Xp22.3 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Chromosome Xp22.3 microdeletion syndrome Is a Developmental hereditary disorder false Inferred relationship Existential restriction modifier
Chromosome Xp22.3 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Chromosome Xp22.3 microdeletion syndrome Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 1
Chromosome Xp22.3 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
Chromosome Xp22.3 microdeletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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