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237870002: Familial lichen amyloidosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
356480011 Familial lichen amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module
626661013 Familial lichen amyloidosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial lichen amyloidosis Is a Localized hereditary amyloidosis true Inferred relationship Existential restriction modifier
Familial lichen amyloidosis Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier
Familial lichen amyloidosis Finding site Body system structure false Inferred relationship Existential restriction modifier
Familial lichen amyloidosis Associated morphology Focal amyloid true Inferred relationship Existential restriction modifier 1
Familial lichen amyloidosis Is a Amyloidosis of skin true Inferred relationship Existential restriction modifier
Familial lichen amyloidosis Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Familial lichen amyloidosis Finding site Skin 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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