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32107005: Anomaly of chromosome pair 17 (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
53647017 Anomaly of chromosome pair 17 en Synonym Active Entire term case insensitive SNOMED CT core module
53648010 Anomaly of chromosome pair 17, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
763352014 Anomaly of chromosome pair 17 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

28 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 17 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 17 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 17 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 17 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 17 Finding site Chromosome pair 17 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 17 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 17 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 17 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 17 Finding site Chromosome pair 17 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 17 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 17 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 17 Finding site Chromosome pair 17 true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
17q partial trisomy syndrome Is a False Anomaly of chromosome pair 17 Inferred relationship Existential restriction modifier
17p partial trisomy syndrome Is a False Anomaly of chromosome pair 17 Inferred relationship Existential restriction modifier
Deletion of long arm of chromosome 17 Is a False Anomaly of chromosome pair 17 Inferred relationship Existential restriction modifier
Koolen De Vries syndrome Is a True Anomaly of chromosome pair 17 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 17 Is a True Anomaly of chromosome pair 17 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 17 Is a True Anomaly of chromosome pair 17 Inferred relationship Existential restriction modifier
Mosaic trisomy 17 syndrome Is a True Anomaly of chromosome pair 17 Inferred relationship Existential restriction modifier
Ring chromosome 17 syndrome Is a True Anomaly of chromosome pair 17 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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