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392133001: Pigment dispersion syndrome (disorder)


Status: current, 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
1466313010 Pigment dispersion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1486119014 Pigment dispersion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1466313010 Pigment dispersion syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1466313010 Pigment dispersion syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1486119014 Pigment dispersion syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1486119014 Pigment dispersion syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
608931000274119 Pigmentdispersionssyndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5248821000241118 syndrome de dispersion pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5248821000241118 syndrome de dispersion pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
608931000274119 Pigmentdispersionssyndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pigment dispersion syndrome Is a Disorder of anterior segment of eye (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Pigment dispersion syndrome Finding site Anterior eyeball segment structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigment dispersion syndrome Is a Lesion of iris (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Pigment dispersion syndrome Is a Disorder of pigmentation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Pigment dispersion syndrome Is a Degenerative disorder of eye (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Pigment dispersion syndrome Finding site Structure of pigmented layer of iris true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigment dispersion syndrome Associated morphology Depigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigment dispersion syndrome Associated morphology Structure showing abnormal deposition of pigment (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pigment dispersion syndrome Finding site Anterior eyeball segment structure true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Pigment dispersion syndrome of bilateral eyes (disorder) Is a False Pigment dispersion syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Pigment dispersion syndrome of right eye Is a True Pigment dispersion syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Pigment dispersion syndrome of left eye (disorder) Is a True Pigment dispersion syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Bilateral acute depigmentation of the iris (BADI) is characterised by acute onset of bilateral iris depigmentation, pigment dispersion in the anterior chamber, and heavy pigment deposition in the anterior chamber angle. Patients typically present with acute and usually severe photophobia, blurred vision, red eye, and ocular discomfort or pain with a usually self-limiting clinical course. Cases often occur after a flu-like illness, upper respiratory tract infection, and after the use of oral moxifloxacin. When associated with iris epithelial depigmentation, iris transillumination defects and atonic/mydriatic pupil, the condition is referred to as bilateral acute iris transillumination (BAIT) which has an increased risk of severe intractable rise in intraocular pressure. Is a True Pigment dispersion syndrome Inferred relationship Existential restriction modifier (core metadata concept)
Secondary ocular hypertension due to pigment dispersion syndrome Due to True Pigment dispersion syndrome Inferred relationship Existential restriction modifier (core metadata concept) 2
Ocular hypertension of left eye due to pigment dispersion syndrome (disorder) Due to True Pigment dispersion syndrome Inferred relationship Existential restriction modifier (core metadata concept) 3
Ocular hypertension of right eye due to pigment dispersion syndrome (disorder) Due to True Pigment dispersion syndrome Inferred relationship Existential restriction modifier (core metadata concept) 3
Ocular hypertension of bilateral eyes due to pigment dispersion syndrome (disorder) Due to True Pigment dispersion syndrome Inferred relationship Existential restriction modifier (core metadata concept) 5

This concept is not in any reference sets

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