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698848005: Hereditary retinal dystrophy primarily involving sensory retina (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2981458015 Hereditary retinal dystrophy primarily involving sensory retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981465011 Inherited retinal dystrophy primarily involving sensory retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2981483015 Hereditary retinal dystrophy primarily involving sensory retina (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary retinal dystrophy primarily involving sensory retina est un(e) (attribut) Hereditary retinal dystrophy true Inferred relationship Some
Hereditary retinal dystrophy primarily involving sensory retina localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some
Hereditary retinal dystrophy primarily involving sensory retina morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 1
Hereditary retinal dystrophy primarily involving sensory retina localisation d'une constatation (attribut) structure de la rétine true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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