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44710007: Anomaly of chromosome pair 6 (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
430321000241114 anomalie du chromosome 6 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
74584016 Anomaly of chromosome pair 6 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
781869015 Anomaly of chromosome pair 6 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
893241000172111 anomalie du chromosome 6 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


21 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
anomalie du chromosome 6 (trouble) est un(e) (attribut) Anomaly of sex chromosome false Inferred relationship Some
anomalie du chromosome 6 (trouble) est un(e) (attribut) Anomaly of chromosome pair true Inferred relationship Some
anomalie du chromosome 6 (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
anomalie du chromosome 6 (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
anomalie du chromosome 6 (trouble) localisation d'une constatation (attribut) Chromosome pair 6 (cell structure) false Inferred relationship Some 1
anomalie du chromosome 6 (trouble) survenue (attribut) congénital true Inferred relationship Some 1
anomalie du chromosome 6 (trouble) morphologie associée (attribut) Cellular AND/OR subcellular abnormality true Inferred relationship Some 1
anomalie du chromosome 6 (trouble) localisation d'une constatation (attribut) Chromosome pair 6 (cell structure) true Inferred relationship Some 1
anomalie du chromosome 6 (trouble) localisation d'une constatation (attribut) Sex chromosome (cell structure) false Inferred relationship Some
anomalie du chromosome 6 (trouble) localisation d'une constatation (attribut) Chromosome pair 6 (cell structure) false Inferred relationship Some 1
anomalie du chromosome 6 (trouble) morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some
anomalie du chromosome 6 (trouble) survenue (attribut) congénital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
6q partial trisomy syndrome est un(e) (attribut) False anomalie du chromosome 6 (trouble) Inferred relationship Some
6p partial trisomy syndrome est un(e) (attribut) False anomalie du chromosome 6 (trouble) Inferred relationship Some
Distal monosomy 6p (disorder) est un(e) (attribut) False anomalie du chromosome 6 (trouble) Inferred relationship Some
6p22 microdeletion syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 6 (trouble) Inferred relationship Some
6q25 microdeletion syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 6 (trouble) Inferred relationship Some
6q terminal deletion syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 6 (trouble) Inferred relationship Some
Distal trisomy 6p syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 6 (trouble) Inferred relationship Some
Deletion of part of chromosome 6 (disorder) est un(e) (attribut) True anomalie du chromosome 6 (trouble) Inferred relationship Some
Partial trisomy of chromosome 6 est un(e) (attribut) True anomalie du chromosome 6 (trouble) Inferred relationship Some
Ring chromosome 6 syndrome (disorder) est un(e) (attribut) True anomalie du chromosome 6 (trouble) Inferred relationship Some
Maternal uniparental disomy of chromosome 6 (disorder) est un(e) (attribut) True anomalie du chromosome 6 (trouble) Inferred relationship Some
Paternal uniparental disomy of chromosome 6 est un(e) (attribut) True anomalie du chromosome 6 (trouble) Inferred relationship Some

This concept is not in any reference sets

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