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

440989002: Prothrombin G20210A mutation (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
2789930019 Prothrombin G20210A mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2790283013 Prothrombin G20210A mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Prothrombin G20210A mutation (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
Prothrombin G20210A mutation (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Prothrombin G20210A mutation (disorder) est un(e) (attribut) Hereditary thrombophilia (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Homozygous prothrombin G20210A mutation (disorder) est un(e) (attribut) True Prothrombin G20210A mutation (disorder) Inferred relationship Some
Heterozygous prothrombin G20210A mutation (disorder) est un(e) (attribut) True Prothrombin G20210A mutation (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