FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

191012007: Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
293721011 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders en Synonym Active Initial character case insensitive SNOMED CT core
574662018 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders Pathological process Abnormal immune process true Inferred relationship Some 2
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders Is a Disorder of immune structure true Inferred relationship Some
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders Has definitional manifestation Immune system finding false Inferred relationship Some
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders Is a Common variable agammaglobulinaemia true Inferred relationship Some
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders Is a Hereditary disorder of immune system true Inferred relationship Some
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders Finding site Structure of immune system true Inferred relationship Some 1
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders Occurrence Congenital true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start