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764725008: 9p13 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3654892018 9p13 microdeletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3654893011 Monosomy 9p13 en Synonym Active Entire term case insensitive SNOMED CT core module
3654894017 9p13 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
9p13 microdeletion syndrome Is a 9p partial monosomy syndrome false Inferred relationship Existential restriction modifier
9p13 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
9p13 microdeletion syndrome Finding site Chromosome pair 9 true Inferred relationship Existential restriction modifier 2
9p13 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
9p13 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
9p13 microdeletion syndrome Associated morphology Deletion of short arm true Inferred relationship Existential restriction modifier 1
9p13 microdeletion syndrome Finding site Chromosome pair 9 true Inferred relationship Existential restriction modifier 1
9p13 microdeletion syndrome Is a Deletion of part of chromosome 9 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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