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232049001: Adult vitelliform macular dystrophy (disorder)

Status: current, 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
347699011 Adult vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620064010 Adult vitelliform macular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3641842010 Adult-onset foveomacular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5168734011 AOFMD - adult-onset foveomacular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5168735012 AVMD - adult vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5168736013 Gass disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5168737016 Pseudo-Best disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5168738014 Pseudo-vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5168739018 Adult-onset vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5168733017 A rare genetic macular dystrophy with characteristics of blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated yellow egg yolk-like lesion located in the foveal or parafoveal region. Clinical onset is typically between the fourth and sixth decade of life. The mechanism underlying the physiopathology is unknown. An autosomal dominant inheritance with variable expression and incomplete penetrance is suggested but the disease can also be sporadic without evidence of a familial inheritance pattern. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
347699011 Adult vitelliform macular dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
347699011 Adult vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620064010 Adult vitelliform macular dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
620064010 Adult vitelliform macular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3641842010 Adult-onset foveomacular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5168734011 AOFMD - adult-onset foveomacular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5168735012 AVMD - adult vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5168736013 Gass disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5168737016 Pseudo-Best disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5168738014 Pseudo-vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5168739018 Adult-onset vitelliform macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5168733017 A rare genetic macular dystrophy with characteristics of blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated yellow egg yolk-like lesion located in the foveal or parafoveal region. Clinical onset is typically between the fourth and sixth decade of life. The mechanism underlying the physiopathology is unknown. An autosomal dominant inheritance with variable expression and incomplete penetrance is suggested but the disease can also be sporadic without evidence of a familial inheritance pattern. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
543701000274119 Adulte vitelliforme Makuladystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3433661001000119 Adulte foveomakuläre vitelliforme Dystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6927911000241119 dystrophie maculaire vitelliforme de l'adulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6927911000241119 dystrophie maculaire vitelliforme de l'adulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
543701000274119 Adulte vitelliforme Makuladystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3433661001000119 Adulte foveomakuläre vitelliforme Dystrophie 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
Adult vitelliform macular dystrophy Is a dystrophie vitelliforme false Inferred relationship Existential restriction modifier (core metadata concept)
Adult vitelliform macular dystrophy Finding site Macula lutea structure false Inferred relationship Existential restriction modifier (core metadata concept)
Adult vitelliform macular dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult vitelliform macular dystrophy Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult vitelliform macular dystrophy Finding site Macula lutea structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult vitelliform macular dystrophy Due to Macular vitelliform deposits false Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult vitelliform macular dystrophy Occurrence Adulthood true Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult vitelliform macular dystrophy Is a Macular vitelliform deposits true Inferred relationship Existential restriction modifier (core metadata concept)
Adult vitelliform macular dystrophy Is a Chronic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Adult vitelliform macular dystrophy Is a Retinal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Adult vitelliform macular dystrophy Is a Genetic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Adult vitelliform macular dystrophy Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Adult vitelliform macular dystrophy Occurrence Adulthood true Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult vitelliform macular dystrophy Finding site Macula lutea structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult vitelliform macular dystrophy Associated morphology Deposition true Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult vitelliform macular dystrophy Is a Degenerative disorder of macula (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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