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1003449005: Paternal 14q32.2 microdeletion (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
4164743018 Paternal 14q32.2 microdeletion (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4164744012 Paternal 14q32.2 microdeletion en Synonym Active Entire term case insensitive SNOMED CT core module
4164745013 Paternal monosomy 14q32.2 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
Paternal 14q32.2 microdeletion Is a Deletion of part of chromosome 14 false Inferred relationship Existential restriction modifier
Paternal 14q32.2 microdeletion Is a Congenital malformation false Inferred relationship Existential restriction modifier
Paternal 14q32.2 microdeletion Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Paternal 14q32.2 microdeletion Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Paternal 14q32.2 microdeletion Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Paternal 14q32.2 microdeletion Finding site Chromosome pair 14 true Inferred relationship Existential restriction modifier 1
Paternal 14q32.2 microdeletion Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier 2
Paternal 14q32.2 microdeletion Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 2
Paternal 14q32.2 microdeletion Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Paternal 14q32.2 microdeletion Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Paternal 14q32.2 microdeletion Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
Paternal 14q32.2 microdeletion Is a Partial deletion of long arm of chromosome 14 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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