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890110004: 17q23.1-q23.2 duplication syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4008407010 17q23.1-q23.2 duplication syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4008408017 17q23.1-q23.2 duplication syndrome (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
17q23.1-q23.2 duplication syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
17q23.1-q23.2 duplication syndrome Is a 17q partial trisomy syndrome true Inferred relationship Existential restriction modifier
17q23.1-q23.2 duplication syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 1
17q23.1-q23.2 duplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
17q23.1-q23.2 duplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 1
17q23.1-q23.2 duplication syndrome Finding site Chromosome pair 17 true Inferred relationship Existential restriction modifier 2
17q23.1-q23.2 duplication syndrome Associated morphology Partial trisomy true Inferred relationship Existential restriction modifier 2
17q23.1-q23.2 duplication syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
17q23.1-q23.2 duplication syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier
17q23.1-q23.2 duplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
17q23.1-q23.2 duplication syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
17q23.1-q23.2 duplication syndrome Is a Developmental hereditary disorder 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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