129581007: Congenital dystrophia brevicollis (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

208373012 Congenital dystrophia brevicollis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

208374018 Bonnevie-Ullrich and Klippel-Feil syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

208375017 Klippel-Feil and Turner syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

208376016 Nielsen's disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

733732016 Congenital dystrophia brevicollis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital dystrophia brevicollis	Is a	Autosomal hereditary disorder	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)