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880078001: 11p15 deletion syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3994437010 11p15 deletion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3994438017 11p15 deletion syndrome (disorder) en Fully specified name 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
11p15 deletion syndrome est un(e) (attribut) 11p partial monosomy syndrome (disorder) true Inferred relationship Some
11p15 deletion syndrome est un(e) (attribut) syndrome de malformations multisystémiques true Inferred relationship Some
11p15 deletion syndrome morphologie associée (attribut) Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
11p15 deletion syndrome localisation d'une constatation (attribut) Chromosome pair 11 (cell structure) true Inferred relationship Some 1
11p15 deletion syndrome survenue (attribut) congénital true Inferred relationship Some 1
11p15 deletion syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
11p15 deletion syndrome localisation d'une constatation (attribut) Chromosome pair 11 (cell structure) true Inferred relationship Some 2
11p15 deletion syndrome morphologie associée (attribut) Deletion of short arm true Inferred relationship Some 2
11p15 deletion syndrome survenue (attribut) congénital true Inferred relationship Some 2
11p15 deletion syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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