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782877002: Xp22.13p22.2 duplication syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3756515014 Xp22.13p22.2 duplication syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3756516010 Xp22.13p22.2 duplication syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Xp22.13p22.2 duplication syndrome Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier
Xp22.13p22.2 duplication syndrome Is a Duplication of chromosome true Inferred relationship Existential restriction modifier
Xp22.13p22.2 duplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
Xp22.13p22.2 duplication syndrome Is a Developmental delay true Inferred relationship Existential restriction modifier
Xp22.13p22.2 duplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Xp22.13p22.2 duplication syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Xp22.13p22.2 duplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Xp22.13p22.2 duplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 2
Xp22.13p22.2 duplication syndrome Finding site Sex chromosome X true Inferred relationship Existential restriction modifier 2
Xp22.13p22.2 duplication syndrome Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 1
Xp22.13p22.2 duplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Xp22.13p22.2 duplication syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Xp22.13p22.2 duplication syndrome Is a X-linked recessive hereditary disease 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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