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27183007: Anomaly of chromosome pair 14 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1007091000172117 anomalie du chromosome 14 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
411601000241111 anomalie du chromosome 14 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
45457017 Anomaly of chromosome pair 14 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
757721014 Anomaly of chromosome pair 14 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


25 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
anomalie du chromosome 14 est un(e) (attribut) Anomaly of sex chromosome false Inferred relationship Some
anomalie du chromosome 14 est un(e) (attribut) Anomaly of chromosome pair true Inferred relationship Some
anomalie du chromosome 14 morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
anomalie du chromosome 14 morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
anomalie du chromosome 14 localisation d'une constatation (attribut) Chromosome pair 14 false Inferred relationship Some 1
anomalie du chromosome 14 survenue (attribut) congénital true Inferred relationship Some 1
anomalie du chromosome 14 morphologie associée (attribut) Cellular AND/OR subcellular abnormality true Inferred relationship Some 1
anomalie du chromosome 14 localisation d'une constatation (attribut) Chromosome pair 14 true Inferred relationship Some 1
anomalie du chromosome 14 morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some
anomalie du chromosome 14 localisation d'une constatation (attribut) Sex chromosome (cell structure) false Inferred relationship Some
anomalie du chromosome 14 survenue (attribut) congénital false Inferred relationship Some
anomalie du chromosome 14 localisation d'une constatation (attribut) Chromosome pair 14 false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Maternal uniparental disomy of chromosome 14 est un(e) (attribut) True anomalie du chromosome 14 Inferred relationship Some
Paternal uniparental disomy of chromosome 14 est un(e) (attribut) True anomalie du chromosome 14 Inferred relationship Some
Ring chromosome 14 syndrome (disorder) est un(e) (attribut) True anomalie du chromosome 14 Inferred relationship Some
Complete trisomy 14 syndrome est un(e) (attribut) False anomalie du chromosome 14 Inferred relationship Some
14q partial trisomy (disorder) est un(e) (attribut) False anomalie du chromosome 14 Inferred relationship Some
14q11.2 microdeletion syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 14 Inferred relationship Some
14q12 microdeletion syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 14 Inferred relationship Some
Deletion of part of chromosome 14 (disorder) est un(e) (attribut) True anomalie du chromosome 14 Inferred relationship Some
Partial trisomy of chromosome 14 (disorder) est un(e) (attribut) True anomalie du chromosome 14 Inferred relationship Some
Mosaic trisomy 14 syndrome (disorder) est un(e) (attribut) True anomalie du chromosome 14 Inferred relationship Some

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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