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766766005: 1p31p32 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
3662550015 1p31p32 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3662551016 Monosomy 1p31p32 en Synonym Active Entire term case insensitive SNOMED CT core module
3662552011 1p31p32 microdeletion 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
1p31p32 microdeletion syndrome Is a 1p partial monosomy true Inferred relationship Existential restriction modifier
1p31p32 microdeletion syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 1
1p31p32 microdeletion syndrome Finding site Chromosome pair 1 true Inferred relationship Existential restriction modifier 2
1p31p32 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
1p31p32 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
1p31p32 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
1p31p32 microdeletion syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 2
1p31p32 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
1p31p32 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
1p31p32 microdeletion syndrome Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 1
1p31p32 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
1p31p32 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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