FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

21877004: Osler hemorrhagic telangiectasia syndrome (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
3394008012 maladie de Rendu-Osler fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
36695013 Osler hemorrhagic telangiectasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
36696014 Osler-Weber-Rendu disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
36697017 Hereditary hemorrhagic telangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
405711000241118 maladie de Rendu-Osler (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
481146013 Osler-Rendu-Weber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
481147016 Osler-Rendu-Weber disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
481148014 Osler haemorrhagic telangiectasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
481149018 Hereditary haemorrhagic telangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
481150018 HHT - Hereditary haemorrhagic telangiectasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
481151019 HHT - Hereditary hemorrhagic telangiectasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
751221018 Osler hemorrhagic telangiectasia syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
maladie de Rendu-Osler survenue (attribut) congénital true Inferred relationship Some 1
maladie de Rendu-Osler Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
maladie de Rendu-Osler est un(e) (attribut) Congenital anomaly of skin false Inferred relationship Some
maladie de Rendu-Osler Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
maladie de Rendu-Osler morphologie associée (attribut) malformation artérioveineuse (anomalie morphologique) true Inferred relationship Some 3
maladie de Rendu-Osler est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
maladie de Rendu-Osler est un(e) (attribut) Congenital venous malformation of skin (disorder) false Inferred relationship Some
maladie de Rendu-Osler est un(e) (attribut) malformation artérioveineuse congénitale true Inferred relationship Some
maladie de Rendu-Osler Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
maladie de Rendu-Osler est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
maladie de Rendu-Osler localisation d'une constatation (attribut) Blood vessel structure (body structure) true Inferred relationship Some 1
maladie de Rendu-Osler localisation d'une constatation (attribut) structure du système vasculaire périphérique false Inferred relationship Some
maladie de Rendu-Osler est un(e) (attribut) télangiectasies true Inferred relationship Some
maladie de Rendu-Osler est un(e) (attribut) Congenital anomaly of integument false Inferred relationship Some
maladie de Rendu-Osler est un(e) (attribut) Skin lesion false Inferred relationship Some
maladie de Rendu-Osler est un(e) (attribut) Congenital hamartosis false Inferred relationship Some
maladie de Rendu-Osler localisation d'une constatation (attribut) Microscopic skin vascular structure false Inferred relationship Some 1
maladie de Rendu-Osler morphologie associée (attribut) Hamartoma (morphologic abnormality) false Inferred relationship Some
maladie de Rendu-Osler localisation d'une constatation (attribut) Microscopic skin vascular structure false Inferred relationship Some 1
maladie de Rendu-Osler morphologie associée (attribut) Telangiectasis false Inferred relationship Some 1
maladie de Rendu-Osler est un(e) (attribut) Hereditary disorder of the integument false Inferred relationship Some
maladie de Rendu-Osler est un(e) (attribut) Hereditary dysplasia of blood vessel (disorder) true Inferred relationship Some
maladie de Rendu-Osler est un(e) (attribut) Congenital hamartoma (disorder) false Inferred relationship Some
maladie de Rendu-Osler survenue (attribut) congénital false Inferred relationship Some 2
maladie de Rendu-Osler morphologie associée (attribut) Hamartoma (morphologic abnormality) false Inferred relationship Some 2
maladie de Rendu-Osler est un(e) (attribut) Skin lesion false Inferred relationship Some
maladie de Rendu-Osler localisation d'une constatation (attribut) Blood vessel structure (body structure) true Inferred relationship Some 3
maladie de Rendu-Osler survenue (attribut) congénital true Inferred relationship Some 3
maladie de Rendu-Osler morphologie associée (attribut) Telangiectasis false Inferred relationship Some 3
maladie de Rendu-Osler localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 3
maladie de Rendu-Osler survenue (attribut) congénital false Inferred relationship Some
maladie de Rendu-Osler morphologie associée (attribut) Telangiectasis true Inferred relationship Some 1
maladie de Rendu-Osler localisation d'une constatation (attribut) Blood vessel structure (body structure) false Inferred relationship Some
maladie de Rendu-Osler localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Juvenile polyposis syndrome with hereditary haemorrhagic telangiectasia est un(e) (attribut) True maladie de Rendu-Osler Inferred relationship Some
Hereditary hemorrhagic telangiectasia of gingiva est un(e) (attribut) True maladie de Rendu-Osler Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start