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1231757001: Idiopathic optic perineuritis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5074146011 Idiopathic optic perineuritis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5074147019 Idiopathic optic perineuritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400214015 A rare ophthalmic disorder characterized by idiopathic orbital inflammation in which the specific target tissue is the optic nerve sheath. Patients typically present with ocular pain, pain on eye movement, visual symptoms with loss of vision progressing over several weeks, dyschromatopsia, and variable visual field defects. Orbital signs and symptoms may be present and include ptosis, ophthalmoplegia, and exophthalmos. Optic disc edema is observed in most cases. The condition is usually unilateral. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400215019 A rare ophthalmic disorder characterised by idiopathic orbital inflammation in which the specific target tissue is the optic nerve sheath. Patients typically present with ocular pain, pain on eye movement, visual symptoms with loss of vision progressing over several weeks, dyschromatopsia, and variable visual field defects. Orbital signs and symptoms may be present and include ptosis, ophthalmoplegia, and exophthalmos. Optic disc oedema is observed in most cases. The condition is usually unilateral. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5074146011 Idiopathic optic perineuritis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5074147019 Idiopathic optic perineuritis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5074151017 A rare ophthalmic disorder with characteristics of idiopathic orbital inflammation in which the specific target tissue is the optic nerve sheath. Patients typically present with ocular pain, pain on eye movement, visual symptoms with loss of vision progressing over several weeks, dyschromatopsia and variable visual field defects. Orbital signs and symptoms may be present and include ptosis, ophthalmoplegia, and exophthalmos. Optic disc oedema is observed in most cases. The condition is usually unilateral. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5074152012 A rare ophthalmic disorder with characteristics of idiopathic orbital inflammation in which the specific target tissue is the optic nerve sheath. Patients typically present with ocular pain, pain on eye movement, visual symptoms with loss of vision progressing over several weeks, dyschromatopsia and variable visual field defects. Orbital signs and symptoms may be present and include ptosis, ophthalmoplegia, and exophthalmos. Optic disc edema is observed in most cases. The condition is usually unilateral. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400214015 A rare ophthalmic disorder characterized by idiopathic orbital inflammation in which the specific target tissue is the optic nerve sheath. Patients typically present with ocular pain, pain on eye movement, visual symptoms with loss of vision progressing over several weeks, dyschromatopsia, and variable visual field defects. Orbital signs and symptoms may be present and include ptosis, ophthalmoplegia, and exophthalmos. Optic disc edema is observed in most cases. The condition is usually unilateral. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400215019 A rare ophthalmic disorder characterised by idiopathic orbital inflammation in which the specific target tissue is the optic nerve sheath. Patients typically present with ocular pain, pain on eye movement, visual symptoms with loss of vision progressing over several weeks, dyschromatopsia, and variable visual field defects. Orbital signs and symptoms may be present and include ptosis, ophthalmoplegia, and exophthalmos. Optic disc oedema is observed in most cases. The condition is usually unilateral. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
529841000274112 Idiopathische OPN de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
565361000274114 Idiopathische Optikusperineuritis de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
529841000274112 Idiopathische OPN de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
565361000274114 Idiopathische Optikusperineuritis de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3412241001000115 Optikusperineuritis, idiopathische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Idiopathic optic perineuritis Is a Idiopathic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic optic perineuritis Is a Optic perineuritis true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic optic perineuritis Finding site Optic nerve sheath structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic optic perineuritis Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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