277945007: Schprintzen (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

414694017 Schprintzen en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

671041015 Schprintzen (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Schprintzen	Is a	Craniosynostosis syndrome	false	Inferred relationship	Some
Schprintzen	Occurrence	Congenital	false	Inferred relationship	Some
Schprintzen	Finding site	Joint structure of suture of skull	false	Inferred relationship	Some	2
Schprintzen	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	2
Schprintzen	Finding site	Bone structure of cranium	false	Inferred relationship	Some	1
Schprintzen	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
Schprintzen	Finding site	Joint structure of suture of skull	false	Inferred relationship	Some	2
Schprintzen	Associated morphology	Congenital premature fusion	false	Inferred relationship	Some	2
Schprintzen	Finding site	Bone structure of cranium	false	Inferred relationship	Some
Schprintzen	Finding site	Joint structure of suture of skull	false	Inferred relationship	Some	2
Schprintzen	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
Schprintzen	Associated morphology	Congenital premature fusion	false	Inferred relationship	Some	2
Schprintzen	Finding site	Joint structure of suture of skull	false	Inferred relationship	Some	4
Schprintzen	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	3
Schprintzen	Finding site	Joint structure of suture of skull	false	Inferred relationship	Some	3
Schprintzen	Occurrence	Congenital	false	Inferred relationship	Some	4
Schprintzen	Associated morphology	Congenital premature fusion	false	Inferred relationship	Some	4

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)