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702398007: Hyperferritinemia cataract syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2994983013 Hereditary hyperferritinemia-cataract syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2995014019 Hyperferritinemia cataract syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2995493017 Hyperferritinemia cataract syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2995902012 Bonneau-Beaumont syndrome 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
Hyperferritinemia cataract syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Hyperferritinemia cataract syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Hyperferritinemia cataract syndrome Is a Cataract true Inferred relationship Existential restriction modifier
Hyperferritinemia cataract syndrome Associated with Serum ferritin above reference range true Inferred relationship Existential restriction modifier 2
Hyperferritinemia cataract syndrome Associated morphology Cataract false Inferred relationship Existential restriction modifier 2
Hyperferritinemia cataract syndrome Finding site Structure of lens of eye false Inferred relationship Existential restriction modifier 2
Hyperferritinemia cataract syndrome Finding site Structure of lens of eye true Inferred relationship Existential restriction modifier 1
Hyperferritinemia cataract syndrome Associated morphology Abnormally opaque structure 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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