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361199007: Lattice corneal dystrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
477683013 Familial amyloid neuropathy, Finnish type en Synonym Inactive Only initial character case insensitive SNOMED CT core module
477684019 Finnish type amyloidosis en Synonym Inactive Entire term case sensitive SNOMED CT core module
477685018 Amyloid cranial neuropathy with lattice corneal dystrophy en Synonym Inactive Only initial character case insensitive SNOMED CT core module
477686017 Familial amyloid polyneuropathy type V en Synonym Inactive Only initial character case insensitive SNOMED CT core module
477687014 Amyloid corneal dystrophy en Synonym Inactive Only initial character case insensitive SNOMED CT core module
477688016 Finland type amyloidosis en Synonym Inactive Entire term case sensitive SNOMED CT core module
477689012 Meretoja type amyloidosis en Synonym Inactive Entire term case sensitive SNOMED CT core module
743196010 Lattice corneal dystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2693123015 Lattice corneal dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lattice corneal dystrophy Is a Stromal corneal dystrophy true Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Finding site Structure of substantia propria of cornea true Inferred relationship Existential restriction modifier 1
Lattice corneal dystrophy Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Is a Familial amyloid neuropathy, Finnish type false Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Is a Hereditary corneal dystrophy true Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Finding site Nerve structure false Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier 2
Lattice corneal dystrophy Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier 2
Lattice corneal dystrophy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 1
Lattice corneal dystrophy Finding site Structure of substantia propria of cornea false Inferred relationship Existential restriction modifier 1
Lattice corneal dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Lattice corneal dystrophy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier 2
Lattice corneal dystrophy Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier 2
Lattice corneal dystrophy Finding site Peripheral nerve structure false Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Finding site Structure of substantia propria of cornea true Inferred relationship Existential restriction modifier 2
Lattice corneal dystrophy Is a Corneal deposit false Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Is a Ocular amyloid deposit false Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Is a Hereditary amyloidosis false Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Is a Localized hereditary amyloidosis true Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Is a Amyloid of cornea true Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Associated morphology Focal amyloid true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Lattice corneal dystrophy Type I Is a True Lattice corneal dystrophy Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Type II Is a False Lattice corneal dystrophy Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Type III Is a False Lattice corneal dystrophy Inferred relationship Existential restriction modifier
Lattice dystrophy of substantia propria of cornea of bilateral eyes Is a True Lattice corneal dystrophy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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