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78740005: Complete monosomy 21 (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4555287013 Complete monosomy 21 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4555288015 Complete monosomy 21 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete monosomy 21 (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Complete monosomy 21 (disorder) est un(e) (attribut) Monosomy and deletion from autosome false Inferred relationship Some
Complete monosomy 21 (disorder) est un(e) (attribut) anomalie du chromosome 21 true Inferred relationship Some
Complete monosomy 21 (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
Complete monosomy 21 (disorder) localisation d'une constatation (attribut) Chromosome pair 21 (cell structure) false Inferred relationship Some 1
Complete monosomy 21 (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Complete monosomy 21 (disorder) localisation d'une constatation (attribut) Chromosome pair 21 (cell structure) true Inferred relationship Some 1
Complete monosomy 21 (disorder) morphologie associée (attribut) Monosomy true Inferred relationship Some 1
Complete monosomy 21 (disorder) est un(e) (attribut) Complete monosomy of autosome (disorder) true Inferred relationship Some
Complete monosomy 21 (disorder) localisation d'une constatation (attribut) Chromosome pair 21 (cell structure) false Inferred relationship Some 1
Complete monosomy 21 (disorder) morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some
Complete monosomy 21 (disorder) morphologie associée (attribut) Monosomy false Inferred relationship Some
Complete monosomy 21 (disorder) survenue (attribut) congénital false Inferred relationship Some
Complete monosomy 21 (disorder) localisation d'une constatation (attribut) Sex chromosome (cell structure) false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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