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1187119002: hereditaire Behçet-achtige ziekte op kinderleeftijd (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4669941019 Behçet-like disease due to HA20 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4669942014 Hereditary paediatric Behçet-like disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4669943016 Hereditary pediatric Behçet-like disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4669944010 Hereditary pediatric Behçet-like disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4669945011 Behçet-like disease due to haploinsufficiency of A20 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
13252691000146111 op oculo-urogenitaal syndroom lijkende ziekte door haplo-insufficiëntie van A20 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13252701000146111 Behçet-achtige ziekte door HA20 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13307361000146112 hereditaire Behçet-achtige ziekte op kinderleeftijd (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13307371000146118 erfelijke pediatrische Behçet-achtige ziekte nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13307381000146116 hereditaire Behçet-achtige ziekte op kinderleeftijd nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary paediatric Behçet-like disease Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary paediatric Behçet-like disease Is a Inflammatory disorder false Inferred relationship Some
Hereditary paediatric Behçet-like disease Is a Systemic disease false Inferred relationship Some
Hereditary paediatric Behçet-like disease Is a Recurrent disease true Inferred relationship Some
Hereditary paediatric Behçet-like disease Clinical course Recurrent true Inferred relationship Some 3
Hereditary paediatric Behçet-like disease Associated morphology Inflammatory morphology (morphologic abnormality) false Inferred relationship Some 1
Hereditary paediatric Behçet-like disease Is a Haploinsufficiency of A20 true Inferred relationship Some
Hereditary paediatric Behçet-like disease Is a Hereditary disorder of immune system true Inferred relationship Some
Hereditary paediatric Behçet-like disease Finding site Structure of immune system (body structure) true Inferred relationship Some 2
Hereditary paediatric Behçet-like disease Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 2
Hereditary paediatric Behçet-like disease 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

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