232049001: Adult vitelliform macular dystrophy (disorder)

\Retinal dystrophy\Adult vitelliform macular dystrophy

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

11336691000172116 dystrophie maculaire vitelliforme de l'adulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

11336701000172116 dystrophie maculaire vitelliforme chez l'adulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4924831000172113 op volwassen leeftijd optredende vitelliforme maculadystrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Adult vitelliform macular dystrophy	Is a	dystrophie vitelliforme	false	Inferred relationship	Some
Adult vitelliform macular dystrophy	Finding site	Macula lutea structure	false	Inferred relationship	Some
Adult vitelliform macular dystrophy	Associated morphology	Dystrophy	true	Inferred relationship	Some	1
Adult vitelliform macular dystrophy	Finding site	Retinal structure	false	Inferred relationship	Some	1
Adult vitelliform macular dystrophy	Finding site	Macula lutea structure	true	Inferred relationship	Some	1
Adult vitelliform macular dystrophy	Due to	Macular vitelliform deposits	false	Inferred relationship	Some	2
Adult vitelliform macular dystrophy	Occurrence	Adulthood	true	Inferred relationship	Some	1
Adult vitelliform macular dystrophy	Is a	Macular vitelliform deposits	true	Inferred relationship	Some
Adult vitelliform macular dystrophy	Is a	Chronic disease	true	Inferred relationship	Some
Adult vitelliform macular dystrophy	Is a	Retinal dystrophy	true	Inferred relationship	Some
Adult vitelliform macular dystrophy	Is a	Genetic disease	true	Inferred relationship	Some
Adult vitelliform macular dystrophy	Clinical course	Progressive (qualifier value)	true	Inferred relationship	Some	3
Adult vitelliform macular dystrophy	Occurrence	Adulthood	true	Inferred relationship	Some	2
Adult vitelliform macular dystrophy	Finding site	Macula lutea structure	true	Inferred relationship	Some	2
Adult vitelliform macular dystrophy	Associated morphology	Deposition	true	Inferred relationship	Some	2

Inbound Relationships

Characteristic

Refinability

Reference Sets

Belgian GP subset (foundation metadata concept)

Belgian subset for medical problems in patient health records

Description inactivation indicator reference set

GB English

US English

Back to Start

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
11336691000172116	dystrophie maculaire vitelliforme de l'adulte	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
11336701000172116	dystrophie maculaire vitelliforme chez l'adulte	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4924831000172113	op volwassen leeftijd optredende vitelliforme maculadystrofie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)