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2893009: Anomaly of chromosome pair 10 (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
5897015 Anomaly of chromosome pair 10 en Synonym Active Entire term case insensitive SNOMED CT core module
759666019 Anomaly of chromosome pair 10 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

22 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 10 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 10 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 10 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 10 Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 10 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 10 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 10 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 10 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 10 Finding site Chromosome pair 10 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 10 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 10 Finding site Chromosome pair 10 true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 10 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
10q partial monosomy Is a False Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
10p partial trisomy syndrome Is a False Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
10p partial monosomy syndrome Is a False Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
10q partial trisomy syndrome Is a False Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
Complete trisomy 10 syndrome Is a False Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
Ring chromosome 10 syndrome Is a True Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
Trisomy 10p Is a False Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 10 Is a True Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 10 Is a False Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier
Trisomy 10 Is a True Anomaly of chromosome pair 10 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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