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16569009: Anomaly of chromosome pair 15 (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
28033019 Anomaly of chromosome pair 15 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
743616010 Anomaly of chromosome pair 15 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
28033019 Anomaly of chromosome pair 15 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
28033019 Anomaly of chromosome pair 15 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
743616010 Anomaly of chromosome pair 15 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
743616010 Anomaly of chromosome pair 15 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
957771000172115 anomalie du chromosome 15 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
957771000172115 anomalie du chromosome 15 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

22 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 15 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 15 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 15 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 15 Finding site Chromosome pair 15 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 15 Finding site Sex chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 15 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 15 Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 15 Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 15 Finding site Chromosome pair 15 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 15 Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 15 Finding site Chromosome pair 15 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 15 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
15q partial monosomy syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
15q partial trisomy syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Angelman syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Prader-Willi syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
15q13.3 microdeletion Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
15q24 microdeletion Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
15q14 microdeletion syndrome (disorder) Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Isodicentric chromosome 15 syndrome Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 15 (disorder) Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Partial trisomy of chromosome 15 (disorder) Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Ring chromosome 15 syndrome Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Mosaic trisomy 15 syndrome Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Maternal uniparental disomy of chromosome 15 (disorder) Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Paternal uniparental disomy of chromosome 15 Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)
Tetrasomy 15q (disorder) Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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