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237870002: Familial lichen amyloidosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
356480011 Familial lichen amyloidosis en Synonym Active Case insensitive SNOMED CT core
626661013 Familial lichen amyloidosis (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
Familial lichen amyloidosis Is a Amyloidosis of skin true Inferred relationship Some
Familial lichen amyloidosis Is a Hereditary disorder of the integument true Inferred relationship Some
Familial lichen amyloidosis Finding site Skin structure true Inferred relationship Some 1
Familial lichen amyloidosis Associated morphology Focal amyloid true Inferred relationship Some 1
Familial lichen amyloidosis Associated morphology Amyloid deposition false Inferred relationship Some
Familial lichen amyloidosis Finding site Body system structure false Inferred relationship Some
Familial lichen amyloidosis 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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