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698253007: Ultraviolet sensitive syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2973010018 Ultraviolet sensitive syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2973029012 Ultraviolet sensitive syndrome en Synonym Active Case insensitive SNOMED CT core
2973134013 UV sensitive syndrome en Synonym Active Case sensitive SNOMED CT core
2973136010 UVSS - ultraviolet sensitive syndrome en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ultraviolet sensitive syndrome Is a Disorders of skin caused by physical agents true Inferred relationship Some
Ultraviolet sensitive syndrome Causative agent Ultraviolet radiation true Inferred relationship Some 1
Ultraviolet sensitive syndrome Finding site Skin structure true Inferred relationship Some 1
Ultraviolet sensitive syndrome Is a Photosensitivity true Inferred relationship Some
Ultraviolet sensitive syndrome Is a Hereditary disorder of the integument true Inferred relationship Some
Ultraviolet sensitive syndrome Is a Light and ultraviolet-induced dermatosis false Inferred relationship Some
Ultraviolet sensitive syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Ultraviolet sensitive syndrome Causative agent Light and ultraviolet light radiation false Inferred relationship Some
Ultraviolet sensitive syndrome Finding site Skin structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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