56848002: Foville-Wilson syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module

94537010 Foville-Wilson syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

795405011 Foville-Wilson syndrome (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
Foville-Wilson syndrome	Is a	Disorder of brain stem (disorder)	false	Inferred relationship	Some
Foville-Wilson syndrome	Is a	Disorders characterised by eye movement abnormalities that are the result of brain, cranial nerve, or neuromuscular junction dysfunction.	false	Inferred relationship	Some
Foville-Wilson syndrome	Finding site	The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways	false	Inferred relationship	Some
Foville-Wilson syndrome	Finding site	Pontine structure	false	Inferred relationship	Some	1
Foville-Wilson syndrome	Finding site	Eye region structure (body structure)	false	Inferred relationship	Some
Foville-Wilson syndrome	Finding site	The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways	false	Inferred relationship	Some	2
Foville-Wilson syndrome	Interprets	Ocular motility observable	false	Inferred relationship	Some
Foville-Wilson syndrome	Has interpretation	Abnormal	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)