51430000: Cranio-orbito-ocular dysraphia syndrome (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

789328018 Cranio-orbito-ocular dysraphia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

85659013 Cranio-orbito-ocular dysraphia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

85660015 Blatt's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cranio-orbito-ocular dysraphia syndrome (disorder)	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
Cranio-orbito-ocular dysraphia syndrome (disorder)	morphologie associée (attribut)	structure anormale sur le plan morphologique	false	Inferred relationship	Some	1
Cranio-orbito-ocular dysraphia syndrome (disorder)	est un(e) (attribut)	Multiple malformation syndrome with facial defects as major feature	false	Inferred relationship	Some
Cranio-orbito-ocular dysraphia syndrome (disorder)	survenue (attribut)	congénital	false	Inferred relationship	Some	1
Cranio-orbito-ocular dysraphia syndrome (disorder)	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	1
Cranio-orbito-ocular dysraphia syndrome (disorder)	localisation d'une constatation (attribut)	face	false	Inferred relationship	Some	1
Cranio-orbito-ocular dysraphia syndrome (disorder)	morphologie associée (attribut)	Developmental failure of fusion (morphologic abnormality)	false	Inferred relationship	Some	2
Cranio-orbito-ocular dysraphia syndrome (disorder)	survenue (attribut)	congénital	false	Inferred relationship	Some
Cranio-orbito-ocular dysraphia syndrome (disorder)	morphologie associée (attribut)	Congenital failure of fusion	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)