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783160006: Hereditary gelsolin amyloidosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3757887011 Hereditary gelsolin amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module
3757888018 Familial amyloidosis Finnish type en Synonym Active Only initial character case insensitive SNOMED CT core module
3757889014 AGel amyloidosis en Synonym Active Entire term case sensitive SNOMED CT core module
3757890017 Hereditary amyloidosis Finnish type en Synonym Active Only initial character case insensitive SNOMED CT core module
3757891018 Familial amyloid polyneuropathy type IV en Synonym Active Only initial character case insensitive SNOMED CT core module
3757892013 Hereditary gelsolin amyloidosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3757893015 Gelsolin amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module
3788703014 Lattice corneal dystrophy type II en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary gelsolin amyloidosis Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier 4
Hereditary gelsolin amyloidosis Is a Hereditary corneal dystrophy true Inferred relationship Existential restriction modifier
Hereditary gelsolin amyloidosis Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary gelsolin amyloidosis Is a Ocular amyloid deposit true Inferred relationship Existential restriction modifier
Hereditary gelsolin amyloidosis Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Hereditary gelsolin amyloidosis Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Hereditary gelsolin amyloidosis Finding site Structure of eye proper true Inferred relationship Existential restriction modifier 4
Hereditary gelsolin amyloidosis Is a Hereditary amyloidosis true Inferred relationship Existential restriction modifier
Hereditary gelsolin amyloidosis Is a Systemic amyloidosis affecting skin true Inferred relationship Existential restriction modifier
Hereditary gelsolin amyloidosis Finding site Structure of nervous system true Inferred relationship Existential restriction modifier 3
Hereditary gelsolin amyloidosis Finding site Corneal structure true Inferred relationship Existential restriction modifier 1
Hereditary gelsolin amyloidosis Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Hereditary gelsolin amyloidosis Associated morphology Focal amyloid true Inferred relationship Existential restriction modifier 2
Hereditary gelsolin amyloidosis Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier 3
Hereditary gelsolin amyloidosis Finding site Skin structure true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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