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5051002: congenitale anomalie van chromosomenpaar 9 (aandoening)


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
9456010 Anomaly of chromosome pair 9 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
9457018 Anomaly of chromosome pair 9, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
788307018 Anomaly of chromosome pair 9 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6178171000146110 congenitale anomalie van chromosomenpaar 9 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6178181000146112 congenitale anomalie van chromosomenpaar 9 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6178191000146114 aangeboren afwijking van chromosomenpaar 9 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


31 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 9 Is a Anomaly of sex chromosome false Inferred relationship Some
Anomaly of chromosome pair 9 Finding site Sex chromosome false Inferred relationship Some
Anomaly of chromosome pair 9 Occurrence Congenital false Inferred relationship Some
Anomaly of chromosome pair 9 Finding site Chromosome pair 9 false Inferred relationship Some 1
Anomaly of chromosome pair 9 Associated morphology Alteration of chromosome structure false Inferred relationship Some
Anomaly of chromosome pair 9 Is a Anomaly of chromosome pair true Inferred relationship Some
Anomaly of chromosome pair 9 Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
Anomaly of chromosome pair 9 Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some
Anomaly of chromosome pair 9 Finding site Chromosome pair 9 false Inferred relationship Some 1
Anomaly of chromosome pair 9 Occurrence Congenital true Inferred relationship Some 1
Anomaly of chromosome pair 9 Finding site Chromosome pair 9 true Inferred relationship Some 1
Anomaly of chromosome pair 9 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
9q partial trisomy syndrome (disorder) Is a False Anomaly of chromosome pair 9 Inferred relationship Some
9q partial monosomy syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Some
Ring chromosome 9 syndrome Is a True Anomaly of chromosome pair 9 Inferred relationship Some
9p partial monosomy syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Some
Partial tetrasomy of chromosome 9 (disorder) Is a True Anomaly of chromosome pair 9 Inferred relationship Some
Complete trisomy 9 syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Some
9p partial trisomy syndrome Is a False Anomaly of chromosome pair 9 Inferred relationship Some
Deletion of part of chromosome 9 (disorder) Is a True Anomaly of chromosome pair 9 Inferred relationship Some
Partial trisomy of chromosome 9 (disorder) Is a False Anomaly of chromosome pair 9 Inferred relationship Some
Trisomy 9 Is a True Anomaly of chromosome pair 9 Inferred relationship Some
Maternal uniparental disomy of chromosome 9 Is a True Anomaly of chromosome pair 9 Inferred relationship Some
Frontotemporal dementia due to VCP mutation (disorder) Due to True Anomaly of chromosome pair 9 Inferred relationship Some 3
Frontotemporal dementia due to C9orf72 mutation (disorder) Due to True Anomaly of chromosome pair 9 Inferred relationship Some 3

This concept is not in any reference sets

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