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770667002: dystrophie maculaire occulte (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3701926016 Occult macular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701927013 Occult macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701928015 OCMD - occult macular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701929011 OMD - occult macular dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
769631000241111 dystrophie maculaire occulte (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
943631000172116 OCMD - occult macular dystrophy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
981381000172119 dystrophie maculaire occulte fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3701931019 A rare genetic retinal dystrophy disease with characteristics of bilateral progressive decline of visual acuity due to retinal dysfunction confined only to the macula, associated with normal fundus and fluorescein angiograms and severly attenuated focal macular and multifocal electroretinograms. There is evidence the disease is caused by heterozygous mutation in the RP1L1 gene on chromosome 8p23. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Occult macular dystrophy (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 2
Occult macular dystrophy (disorder) morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 1
Occult macular dystrophy (disorder) est un(e) (attribut) maladie chronique true Inferred relationship Some
Occult macular dystrophy (disorder) localisation d'une constatation (attribut) Macula lutea structure true Inferred relationship Some 1
Occult macular dystrophy (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Occult macular dystrophy (disorder) est un(e) (attribut) Hereditary macular dystrophy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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