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371045000: Translocation Down syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1196341016 Translocation Down syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
1209755010 Translocation Down syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
1228917012 Translocation Down's syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Translocation Down syndrome Is a Anomaly of chromosome pair 21 false Inferred relationship Existential restriction modifier
Translocation Down syndrome Is a Unbalanced translocation and insertion true Inferred relationship Existential restriction modifier
Translocation Down syndrome Finding site Chromosome pair 21 false Inferred relationship Existential restriction modifier 1
Translocation Down syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Translocation Down syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Translocation Down syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Translocation Down syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Translocation Down syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Translocation Down syndrome Finding site Chromosome pair 21 false Inferred relationship Existential restriction modifier 1
Translocation Down syndrome Associated morphology Chromosomal translocation false Inferred relationship Existential restriction modifier 2
Translocation Down syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Translocation Down syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Translocation Down syndrome Finding site Chromosome pair 21 true Inferred relationship Existential restriction modifier 1
Translocation Down syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Translocation Down syndrome Finding site Chromosome pair 21 true Inferred relationship Existential restriction modifier 2
Translocation Down syndrome Associated morphology Trisomy true Inferred relationship Existential restriction modifier 2
Translocation Down syndrome Associated morphology Chromosomal translocation true Inferred relationship Existential restriction modifier 1
Translocation Down syndrome Is a Complete trisomy 21 syndrome true Inferred relationship Existential restriction modifier
Translocation Down syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Translocation Down syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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