FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

29504002: Posterior polymorphous corneal dystrophy (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
49373018 Polymorphous corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1226363016 Posterior polymorphous corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2545495012 Posterior polymorphous corneal dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
49373018 Polymorphous corneal dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
49373018 Polymorphous corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
760406019 Polymorphous corneal dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1226363016 Posterior polymorphous corneal dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1226363016 Posterior polymorphous corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2545495012 Posterior polymorphous corneal dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2545495012 Posterior polymorphous corneal dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
641061000274113 Hintere polymorphe Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
641071000274117 Polymorphe posteriore Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
923541000172112 dystrophie de Schlichting fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
996911000172119 dystrophie cornéenne postérieure polymorphe fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
923541000172112 dystrophie de Schlichting fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
996911000172119 dystrophie cornéenne postérieure polymorphe fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
641061000274113 Hintere polymorphe Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
641071000274117 Polymorphe posteriore Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3453741001000110 Hornhautdystrophie, polymorphe posteriore de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Polymorphous corneal dystrophy Is a Posterior membrane corneal dystrophy false Inferred relationship Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy Finding site Structure of Descemet's membrane false Inferred relationship Existential restriction modifier (core metadata concept) 1
Polymorphous corneal dystrophy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Polymorphous corneal dystrophy Is a Chandler syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy Finding site Structure of corneal endothelium false Inferred relationship Existential restriction modifier (core metadata concept) 1
Polymorphous corneal dystrophy Is a Hereditary corneal dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy Is a Anomaly of chromosome pair 20 false Inferred relationship Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy Is a Corneal endothelial dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Polymorphous corneal dystrophy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Polymorphous corneal dystrophy Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Polymorphous corneal dystrophy Finding site Structure of Descemet's membrane true Inferred relationship Existential restriction modifier (core metadata concept) 1
Polymorphous corneal dystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Polymorphous corneal dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Polymorphous corneal dystrophy Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier (core metadata concept) 2
Polymorphous corneal dystrophy Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 2
Polymorphous corneal dystrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy Is a Descemet's membrane finding true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start