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79656000: Anomaly of chromosome pair 19 (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
132153018 Anomaly of chromosome pair 19 en Synonym Active Entire term case insensitive SNOMED CT core module
820730015 Anomaly of chromosome pair 19 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

13 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 19 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 19 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 19 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 19 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 19 Finding site Chromosome pair 19 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 19 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 19 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 19 Finding site Chromosome pair 19 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 19 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 19 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 19 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 19 Finding site Chromosome pair 19 true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
19q partial trisomy syndrome Is a False Anomaly of chromosome pair 19 Inferred relationship Existential restriction modifier
19p13.12 microdeletion syndrome Is a False Anomaly of chromosome pair 19 Inferred relationship Existential restriction modifier
19q13.11 microdeletion syndrome Is a False Anomaly of chromosome pair 19 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 19 Is a True Anomaly of chromosome pair 19 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 19 Is a True Anomaly of chromosome pair 19 Inferred relationship Existential restriction modifier
Ring chromosome 19 syndrome Is a True Anomaly of chromosome pair 19 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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