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44710007: Anomaly of chromosome pair 6 (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
74584016 Anomaly of chromosome pair 6 en Synonym Active Entire term case insensitive SNOMED CT core module
74585015 Anomaly of chromosome pair 6, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
781869015 Anomaly of chromosome pair 6 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

21 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 6 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 6 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 6 Finding site Chromosome pair 6 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 6 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 6 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 6 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 6 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 6 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 6 Finding site Chromosome pair 6 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 6 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 6 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 6 Finding site Chromosome pair 6 true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
6q partial trisomy syndrome Is a False Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
6p partial trisomy syndrome Is a False Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
Distal monosomy 6p Is a False Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
6p22 microdeletion syndrome Is a False Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
6q25 microdeletion syndrome Is a False Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
6q terminal deletion syndrome Is a False Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
Distal trisomy 6p syndrome Is a False Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 6 Is a True Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 6 Is a True Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
Ring chromosome 6 syndrome Is a True Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
Maternal uniparental disomy of chromosome 6 Is a True Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome 6 Is a True Anomaly of chromosome pair 6 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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