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1187639002: Martinique crinkled retinal pigment epitheliopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4675672010 Martinique crinkled retinal pigment epitheliopathy en Synonym Active Entire term case sensitive SNOMED CT core module
4675673017 Martinique crinkled retinal pigment epitheliopathy (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
4675674011 MCRPE - Martinique crinkled retinal pigment epitheliopathy en Synonym Active Entire term case sensitive SNOMED CT core module


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 Existential restriction modifier
Martinique crinkled retinal pigment epitheliopathy Is a Hereditary macular dystrophy true Inferred relationship Existential restriction modifier
Martinique crinkled retinal pigment epitheliopathy Finding site Macula lutea structure true Inferred relationship Existential restriction modifier 1
Martinique crinkled retinal pigment epitheliopathy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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