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371045000: Translocation Down syndrome (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Chromosomal disorder\Autosomal chromosomal disorder\Autosomal duplication\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome\Translocation Down syndrome
\Chromosomal disorder\Unbalanced translocation and insertion\Translocation Down syndrome
\Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome\Translocation Down syndrome
\Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 21\Complete trisomy 21 syndrome\Translocation Down syndrome
\Chromosomal disorder\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome\Translocation Down syndrome

\Congenital disease\Congenital anomaly\Complete trisomy 21 syndrome\Translocation Down syndrome
\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 21\Complete trisomy 21 syndrome\Translocation Down syndrome
\Congenital disease\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome\Translocation Down syndrome

\Developmental disorder\Congenital anomaly\Complete trisomy 21 syndrome\Translocation Down syndrome

Status: current, Primitive. Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1196341016 Translocation Down syndrome (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

1209755010 Translocation Down syndrome en Synonym Active Initial character case insensitive SNOMED CT core

1228917012 Translocation Down's syndrome en Synonym Active Initial character case insensitive SNOMED CT core

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

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