FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

37535007: Anomaly of chromosome pair 12 (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
422881000241117 anomalie du chromosome 12 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
62616016 Anomaly of chromosome pair 12 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769413013 Anomaly of chromosome pair 12 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
871971000172119 anomalie du chromosome 12 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


22 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
anomalie du chromosome 12 (trouble) est un(e) (attribut) Anomaly of sex chromosome false Inferred relationship Some
anomalie du chromosome 12 (trouble) est un(e) (attribut) Anomaly of chromosome pair true Inferred relationship Some
anomalie du chromosome 12 (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
anomalie du chromosome 12 (trouble) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
anomalie du chromosome 12 (trouble) localisation d'une constatation (attribut) Chromosome pair 12 (cell structure) false Inferred relationship Some 1
anomalie du chromosome 12 (trouble) survenue (attribut) congénital true Inferred relationship Some 1
anomalie du chromosome 12 (trouble) morphologie associée (attribut) Cellular AND/OR subcellular abnormality true Inferred relationship Some 1
anomalie du chromosome 12 (trouble) localisation d'une constatation (attribut) Chromosome pair 12 (cell structure) true Inferred relationship Some 1
anomalie du chromosome 12 (trouble) localisation d'une constatation (attribut) Sex chromosome (cell structure) false Inferred relationship Some
anomalie du chromosome 12 (trouble) survenue (attribut) congénital false Inferred relationship Some
anomalie du chromosome 12 (trouble) localisation d'une constatation (attribut) Chromosome pair 12 (cell structure) false Inferred relationship Some 1
anomalie du chromosome 12 (trouble) morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
12p partial trisomy syndrome est un(e) (attribut) False anomalie du chromosome 12 (trouble) Inferred relationship Some
12p partial monosomy syndrome est un(e) (attribut) False anomalie du chromosome 12 (trouble) Inferred relationship Some
12q partial trisomy syndrome est un(e) (attribut) False anomalie du chromosome 12 (trouble) Inferred relationship Some
tétrasomie 12p (trouble) est un(e) (attribut) True anomalie du chromosome 12 (trouble) Inferred relationship Some
Ulnar mammary syndrome est un(e) (attribut) True anomalie du chromosome 12 (trouble) Inferred relationship Some
12q14 microdeletion syndrome (disorder) est un(e) (attribut) False anomalie du chromosome 12 (trouble) Inferred relationship Some
Deletion of part of chromosome 12 (disorder) est un(e) (attribut) True anomalie du chromosome 12 (trouble) Inferred relationship Some
Partial trisomy of chromosome 12 est un(e) (attribut) False anomalie du chromosome 12 (trouble) Inferred relationship Some
Trisomy 12 est un(e) (attribut) True anomalie du chromosome 12 (trouble) Inferred relationship Some
Ring chromosome 12 syndrome est un(e) (attribut) True anomalie du chromosome 12 (trouble) Inferred relationship Some

This concept is not in any reference sets

Back to Start