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

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

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

3881511000052114 kranioorbitookulärt dysrafisyndrom sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
kranioorbitookulärt dysrafisyndrom	Is a	Multiple malformation syndrome with facial defects as major feature	false	Inferred relationship	Some
kranioorbitookulärt dysrafisyndrom	Occurrence	Congenital	false	Inferred relationship	Some
kranioorbitookulärt dysrafisyndrom	Associated morphology	medfödd utebliven fusion	false	Inferred relationship	Some
kranioorbitookulärt dysrafisyndrom	Occurrence	Congenital	false	Inferred relationship	Some	1
kranioorbitookulärt dysrafisyndrom	Associated morphology	utvecklingsabnormitet	false	Inferred relationship	Some	1
kranioorbitookulärt dysrafisyndrom	Finding site	Face structure	false	Inferred relationship	Some	1
kranioorbitookulärt dysrafisyndrom	Associated morphology	Developmental failure of fusion (morphologic abnormality)	false	Inferred relationship	Some	2
kranioorbitookulärt dysrafisyndrom	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
kranioorbitookulärt dysrafisyndrom	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)