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1187639002: Martinique crinkled retinal pigment epitheliopathy (disorder)


Status: current, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4675672010 Martinique crinkled retinal pigment epitheliopathy en Synonym Active Case sensitive SNOMED CT core
4675673017 Martinique crinkled retinal pigment epitheliopathy (disorder) en Fully specified name Active Case sensitive SNOMED CT core
4675674011 MCRPE - Martinique crinkled retinal pigment epitheliopathy en Synonym Active Case sensitive SNOMED CT core
4675678014 A rare genetic retinal disease with characteristics of dried-out soil pattern of the fundus due to diffuse deep white lines in the macula, to the level of the retinal pigment epithelium, which is slightly elevated and rippled. Macular exudation may be associated and Bruch's membrane may be affected too. Occasionally, peripheral nummular pigmentary changes may be observed, associated with blindness. The lesions enlarge with time, with a preferential macular extension and confluence. Complications may include polypoidal choroidal vasculopathy, choroidal neovascularization or atrophic fibrous macular scarring that can lead to reduced visual acuity over time. en Definition Active Case sensitive SNOMED CT core
4675679018 A rare genetic retinal disease with characteristics of dried-out soil pattern of the fundus due to diffuse deep white lines in the macula, to the level of the retinal pigment epithelium, which is slightly elevated and rippled. Macular exudation may be associated and Bruch's membrane may be affected too. Occasionally, peripheral nummular pigmentary changes may be observed, associated with blindness. The lesions enlarge with time, with a preferential macular extension and confluence. Complications may include polypoidal choroidal vasculopathy, choroidal neovascularisation or atrophic fibrous macular scarring that can lead to reduced visual acuity over time. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Martinique crinkled retinal pigment epitheliopathy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Martinique crinkled retinal pigment epitheliopathy Is a Hereditary macular dystrophy true Inferred relationship Some
Martinique crinkled retinal pigment epitheliopathy Finding site Macula lutea structure true Inferred relationship Some 1
Martinique crinkled retinal pigment epitheliopathy Associated morphology Dystrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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