FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

702398007: Hyperferritinemia cataract syndrome (disorder)


Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2994983013 Hereditary hyperferritinemia-cataract syndrome en Synonym Active Case insensitive SNOMED CT core
2995014019 Hyperferritinemia cataract syndrome en Synonym Active Case insensitive SNOMED CT core
2995493017 Hyperferritinemia cataract syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2995902012 Bonneau-Beaumont syndrome en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperferritinemia cataract syndrome Finding site Structure of lens of eye true Inferred relationship Some 1
Hyperferritinemia cataract syndrome Associated morphology Abnormally opaque structure true Inferred relationship Some 1
Hyperferritinemia cataract syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hyperferritinemia cataract syndrome Is a Hereditary disorder of the visual system 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 Structure of lens of eye false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start