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

154818001: Congenital afibrinogenemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
240815017 Congenital afibrinogenemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
240816016 Congenital afibrinogenaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2788877018 Congenital afibrinogenemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital afibrinogenemia a pour interprétation (attribut) anormal true Inferred relationship Some 2
Congenital afibrinogenemia interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 2
Congenital afibrinogenemia est un(e) (attribut) Hereditary factor I deficiency disease true Inferred relationship Some
Congenital afibrinogenemia survenue (attribut) congénital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start