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32107005: Anomaly of chromosome pair 17 (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
417221000241110 anomalie du chromosome 17 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
53647017 Anomaly of chromosome pair 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
763352014 Anomaly of chromosome pair 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
937001000172114 anomalie du chromosome 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


28 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
anomalie du chromosome 17 (trouble) est un(e) (attribut) Anomaly of sex chromosome false Inferred relationship Some
anomalie du chromosome 17 (trouble) est un(e) (attribut) Anomaly of chromosome pair true Inferred relationship Some
anomalie du chromosome 17 (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
anomalie du chromosome 17 (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
anomalie du chromosome 17 (trouble) localisation d'une constatation (attribut) Chromosome pair 17 (cell structure) false Inferred relationship Some 1
anomalie du chromosome 17 (trouble) survenue (attribut) congénital true Inferred relationship Some 1
anomalie du chromosome 17 (trouble) morphologie associée (attribut) Cellular AND/OR subcellular abnormality true Inferred relationship Some 1
anomalie du chromosome 17 (trouble) localisation d'une constatation (attribut) Chromosome pair 17 (cell structure) true Inferred relationship Some 1
anomalie du chromosome 17 (trouble) localisation d'une constatation (attribut) Sex chromosome (cell structure) false Inferred relationship Some
anomalie du chromosome 17 (trouble) survenue (attribut) congénital false Inferred relationship Some
anomalie du chromosome 17 (trouble) morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some
anomalie du chromosome 17 (trouble) localisation d'une constatation (attribut) Chromosome pair 17 (cell structure) false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Ring chromosome 17 syndrome (disorder) est un(e) (attribut) True anomalie du chromosome 17 (trouble) Inferred relationship Some
17q partial trisomy syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 17 (trouble) Inferred relationship Some
17p partial trisomy syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 17 (trouble) Inferred relationship Some
Deletion of long arm of chromosome 17 (disorder) est un(e) (attribut) False anomalie du chromosome 17 (trouble) Inferred relationship Some
Koolen De Vries syndrome (disorder) est un(e) (attribut) True anomalie du chromosome 17 (trouble) Inferred relationship Some
Deletion of part of chromosome 17 (disorder) est un(e) (attribut) True anomalie du chromosome 17 (trouble) Inferred relationship Some
Partial trisomy of chromosome 17 (disorder) est un(e) (attribut) True anomalie du chromosome 17 (trouble) Inferred relationship Some
Mosaic trisomy 17 syndrome (disorder) est un(e) (attribut) True anomalie du chromosome 17 (trouble) Inferred relationship Some

This concept is not in any reference sets

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