FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

48976006: Prekallikrein deficiency (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
1230668019 Fletcher trait en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
786603018 Prekallikrein deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
81593014 Prekallikrein deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
81594015 Fletcher factor deficiency en Synonym (core metadata concept) 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
Prekallikrein deficiency (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
Prekallikrein deficiency (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Prekallikrein deficiency (disorder) est un(e) (attribut) Contact factor deficiency true Inferred relationship Some
Prekallikrein deficiency (disorder) est un(e) (attribut) Coagulation factor deficiency syndrome true Inferred relationship Some
Prekallikrein deficiency (disorder) localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Prekallikrein deficiency (disorder) est défini par la manifestation de (attribut) constatation sur le système hémostatique false Inferred relationship Some
Prekallikrein deficiency (disorder) localisation d'une constatation (attribut) Entire hematological system (body structure) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
carence en prékallicréine acquise est un(e) (attribut) True Prekallikrein deficiency (disorder) Inferred relationship Some
Hereditary congenital prekallikrein deficiency (disorder) est un(e) (attribut) True Prekallikrein deficiency (disorder) 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