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21877004: Osler hemorrhagic telangiectasia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
36695013 Osler hemorrhagic telangiectasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
36696014 Osler-Weber-Rendu disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
36697017 Hereditary hemorrhagic telangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
481146013 Osler-Rendu-Weber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
481147016 Osler-Rendu-Weber disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
481148014 Osler haemorrhagic telangiectasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
481149018 Hereditary haemorrhagic telangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)
481150018 HHT - Hereditary haemorrhagic telangiectasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
481151019 HHT - Hereditary hemorrhagic telangiectasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)
751221018 Osler hemorrhagic telangiectasia syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osler hemorrhagic telangiectasia syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Osler hemorrhagic telangiectasia syndrome Is a Congenital arteriovenous malformation true Inferred relationship Some
Osler hemorrhagic telangiectasia syndrome Is a Telangiectasia disorder true Inferred relationship Some
Osler hemorrhagic telangiectasia syndrome Is a Hereditary dysplasia of blood vessel (disorder) true Inferred relationship Some
Osler hemorrhagic telangiectasia syndrome Associated morphology Telangiectasis true Inferred relationship Some 1
Osler hemorrhagic telangiectasia syndrome Occurrence Congenital true Inferred relationship Some 1
Osler hemorrhagic telangiectasia syndrome Finding site Blood vessel structure (body structure) true Inferred relationship Some 1
Osler hemorrhagic telangiectasia syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Some 1
Osler hemorrhagic telangiectasia syndrome Associated morphology Arteriovenous malformation true Inferred relationship Some 2
Osler hemorrhagic telangiectasia syndrome Occurrence Congenital true Inferred relationship Some 2
Osler hemorrhagic telangiectasia syndrome Finding site Blood vessel structure (body structure) true Inferred relationship Some 2
Osler hemorrhagic telangiectasia syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

International Patient Summary

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