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361199007: Lattice corneal dystrophy (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
743196010 Lattice corneal dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2693123015 Lattice corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
477683013 Familial amyloid neuropathy, Finnish type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
477684019 Finnish type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
477685018 Amyloid cranial neuropathy with lattice corneal dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
477686017 Familial amyloid polyneuropathy type V en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
477687014 Amyloid corneal dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
477688016 Finland type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
477689012 Meretoja type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
743196010 Lattice corneal dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
743196010 Lattice corneal dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2693123015 Lattice corneal dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2693123015 Lattice corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
557691000274113 Gittrige Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
606991000274119 Gittrige Dystrophie der Kornea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6344601000241112 LCD - lattice corneal dystrophy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6344611000241114 dystrophie cornéenne grillagée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6344601000241112 LCD - lattice corneal dystrophy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6344611000241114 dystrophie cornéenne grillagée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
557691000274113 Gittrige Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
606991000274119 Gittrige Dystrophie der Kornea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Lattice corneal dystrophy Finding site Structure of substantia propria of cornea true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Is a Familial amyloid neuropathy, Finnish type false Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Is a Hereditary corneal dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Finding site Nerve structure false Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Finding site Structure of substantia propria of cornea false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lattice corneal dystrophy Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Finding site Peripheral nerve structure false Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Finding site Structure of substantia propria of cornea true Inferred relationship Existential restriction modifier (core metadata concept) 2
Lattice corneal dystrophy Is a Corneal deposit (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Is a Ocular amyloid deposit false Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Is a Hereditary amyloidosis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Is a Localized hereditary amyloidosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Is a Amyloid of cornea true Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Associated morphology Focal amyloid true Inferred relationship Existential restriction modifier (core metadata concept) 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 (core metadata concept)
Lattice corneal dystrophy Type II Is a False Lattice corneal dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy Type III Is a False Lattice corneal dystrophy Inferred relationship Existential restriction modifier (core metadata concept)
Lattice dystrophy of substantia propria of cornea of bilateral eyes (disorder) Is a True Lattice corneal dystrophy Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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