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237872005: Poikilodermal cutaneous amyloid (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356482015 Poikilodermal cutaneous amyloid en Synonym Active Case insensitive SNOMED CT core
626663011 Poikilodermal cutaneous amyloid (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Poikilodermal cutaneous amyloid Is a Hereditary disorder of the integument true Inferred relationship Some
Poikilodermal cutaneous amyloid Associated morphology Focal amyloid false Inferred relationship Some 1
Poikilodermal cutaneous amyloid Finding site Skin structure true Inferred relationship Some 1
Poikilodermal cutaneous amyloid Associated morphology Focal amyloid true Inferred relationship Some 1
Poikilodermal cutaneous amyloid Finding site Skin structure false Inferred relationship Some 1
Poikilodermal cutaneous amyloid Associated morphology Amyloid deposition false Inferred relationship Some
Poikilodermal cutaneous amyloid Is a Amyloidosis of skin true Inferred relationship Some
Poikilodermal cutaneous amyloid Is a Localised hereditary amyloidosis true 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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