A.39 Spatial Registration IODs

A.39 Spatial Registration IODs (Current)
Prev	A Composite Information Object Definitions (Normative)	Next

The Registration IOD specifies the spatial relationship between Frames of Reference.

This IOD uses the E-R Model in Section A.1.2, with only the Registration IE below the Series IE.

Table A.39.1-1 specifies the Modules of the Spatial Registration IOD.

Table A.39.1-1. Spatial Registration IOD Modules

IE	Module	Reference	Usage
Patient	Patient	C.7.1.1	M
Patient	Clinical Trial Subject	C.7.1.3	U
Study	General Study	C.7.2.1	M
	Patient Study	C.7.2.2	U
	Clinical Trial Study	C.7.2.3	U
Series	General Series	C.7.3.1	M
	Clinical Trial Series	C.7.3.2	U
	Spatial Registration Series	C.20.1	M
Frame of Reference	Frame of Reference	C.7.4.1	M
Equipment	General Equipment	C.7.5.1	M
Spatial Registration	Spatial Registration	C.20.2	M
	Common Instance Reference	C.12.2	M
	General Reference	C.12.4	U
	SOP Common	C.12.1	M

The Specimen Identification Module (Retired) was previously included in this IOD but has been retired. See PS3.3-2008.

Prev	Up	Next
A.38 Enhanced CT Image IODs	Home	A.39.2 Deformable Spatial Registration IOD