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17760001: Anomaly of chromosome pair 13 (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
30013010 Anomaly of chromosome pair 13 en Synonym Active Entire term case insensitive SNOMED CT core module
745100012 Anomaly of chromosome pair 13 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

25 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 13 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 13 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 13 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 13 Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 13 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 13 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 13 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 13 Finding site Chromosome pair 13 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 13 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 13 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 13 Finding site Chromosome pair 13 true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 13 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
13q partial trisomy syndrome Is a False Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
Partial trisomy 13 in Patau's syndrome Is a True Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Is a False Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
13q partial monosomy syndrome Is a False Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
13p partial trisomy syndrome Is a False Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
Complete trisomy 13 syndrome Is a True Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
Ring chromosome 13 syndrome Is a True Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 13 Is a True Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 13 Is a True Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome 13 Is a True Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier
Maternal uniparental disomy of chromosome 13 Is a True Anomaly of chromosome pair 13 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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