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

763623001: ernstige gecombineerde immunodeficiëntie door CTPS1-deficiëntie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3643070016 Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643071017 Severe combined immunodeficiency due to CTPS1 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3643072012 Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6259641000146115 ernstige gecombineerde immuundeficiëntie door CTPS1-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6259661000146119 ernstige gecombineerde immunodeficiëntie door CTPS1-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6259671000146113 'severe combined immunodeficiency' door CTPS1-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6259681000146110 SCID door CTPS1-deficiëntie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6887471000146117 ernstige gecombineerde immunodeficiëntie door CTPS1-deficiëntie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3643073019 A rare primary immunodeficiency disorder due to impaired capacity of activated T and B-cells to proliferate in response to antigen receptor-mediated activation. The disease has characteristics of early-onset severe persistent and/or recurrent viral infections due to Epstein-Barr virus and Varicella Zoster virus as well as recurrent sino-pulmonary bacterial infections due to encapsulated pathogens. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe combined immunodeficiency due to CTPS1 deficiency Is a Severe combined immunodeficiency with low T- and B-cell numbers true Inferred relationship Some
Severe combined immunodeficiency due to CTPS1 deficiency Is a Autosomal recessive severe combined immunodeficiency disease (disorder) true Inferred relationship Some
Severe combined immunodeficiency due to CTPS1 deficiency Finding site Structure of immune system (body structure) true Inferred relationship Some 1
Severe combined immunodeficiency due to CTPS1 deficiency Occurrence Congenital true Inferred relationship Some 1
Severe combined immunodeficiency due to CTPS1 deficiency Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start