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1156858008: Autosomal dominant progressive external ophthalmoplegia type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4576342017 Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4576343010 Autosomal dominant progressive external ophthalmoplegia type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4576342017 Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4576343010 Autosomal dominant progressive external ophthalmoplegia type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591811000274117 adPEO - Autosomal-dominante externe progressive Ophthalmoplegie Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
591821000274112 Autosomal-dominante externe progressive Ophthalmoplegie Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5789091000241116 ophtalmoplégie externe progressive autosomique dominante de type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5789091000241116 ophtalmoplégie externe progressive autosomique dominante de type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
591811000274117 adPEO - Autosomal-dominante externe progressive Ophthalmoplegie Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
591821000274112 Autosomal-dominante externe progressive Ophthalmoplegie Typ 2 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
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Finding site Structure of extraocular muscle true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Is a Autosomal dominant progressive external ophthalmoplegia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 5
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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