90036004: Vitelliform dystrophy (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

149249010 Vitelliform dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

833056010 Vitelliform dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1235526010 Vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

151431000172118 dystrophie vitelliforme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3394441001000119 Best vitelliforme Makuladegeneration de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
dystrophie vitelliforme	Is a	Hereditary macular dystrophy	false	Inferred relationship	Some
dystrophie vitelliforme	Is a	Autosomal dominant hereditary disorder (disorder)	false	Inferred relationship	Some
dystrophie vitelliforme	Finding site	Macula lutea structure	false	Inferred relationship	Some
dystrophie vitelliforme	Associated morphology	Dystrophy	false	Inferred relationship	Some	1
dystrophie vitelliforme	Finding site	Retinal structure	false	Inferred relationship	Some	1
dystrophie vitelliforme	Finding site	Macula lutea structure	false	Inferred relationship	Some	1
dystrophie vitelliforme	Due to	Macular vitelliform deposits	false	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare, genetic, macular dystrophy characterized by blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated, yellow, egg yolk-like lesion located in the foveal or parafoveal region.	Is a	False	dystrophie vitelliforme	Inferred relationship	Some
Best vitelliform macular dystrophy (BVMD) is a genetic macular dystrophy characterized by loss of central visual acuity, metamorphopsia and a decrease in the Arden ratio secondary to an egg yolk-like lesion located in the foveal or parafoveal region.	Is a	False	dystrophie vitelliforme	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)