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702398007: Hyperferritinemia cataract syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2994983013 Hereditary hyperferritinemia-cataract syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995014019 Hyperferritinemia cataract syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995493017 Hyperferritinemia cataract syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995902012 Bonneau-Beaumont syndrome en Synonym (core metadata concept) 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
Hyperferritinemia cataract syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hyperferritinemia cataract syndrome Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Hyperferritinemia cataract syndrome Is a Cataract true Inferred relationship Some
Hyperferritinemia cataract syndrome Associated with Serum ferritin above reference range true Inferred relationship Some 2
Hyperferritinemia cataract syndrome Associated morphology Cataract false Inferred relationship Some 2
Hyperferritinemia cataract syndrome Finding site Lens clear false Inferred relationship Some 2
Hyperferritinemia cataract syndrome Finding site Lens clear true Inferred relationship Some 1
Hyperferritinemia cataract syndrome Associated morphology Opacity 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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