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

238764001: Hereditary benign telangiectasia (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
357850018 Hereditary benign telangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
627688013 Hereditary benign telangiectasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
357850018 Hereditary benign telangiectasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
357850018 Hereditary benign telangiectasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
627688013 Hereditary benign telangiectasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
627688013 Hereditary benign telangiectasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5025411000241113 télangiectasie bénigne héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5025411000241113 télangiectasie bénigne héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary benign telangiectasia Is a Primary idiopathic cutaneous telangiectasia false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary benign telangiectasia Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary benign telangiectasia Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary benign telangiectasia Finding site Peripheral vascular system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary benign telangiectasia Associated morphology Telangiectasis false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary benign telangiectasia Finding site Microscopic skin vascular structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary benign telangiectasia Finding site Microscopic skin vascular structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary benign telangiectasia Associated morphology Telangiectasis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary benign telangiectasia Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary benign telangiectasia Is a Telangiectasia disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary benign telangiectasia Is a Hereditary disorder of the integument (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary benign telangiectasia Finding site Blood vessel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start