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1254946006: Griscelli type 1 (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5143922017 Hypopigmentation-immunodeficiency disease type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5143923010 Griscelli syndrome type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5146507013 Hypopigmentation-immunodeficiency disease type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
14077241000146111 syndroom van Griscelli-Pruniéras type 1 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14077251000146114 Griscelli type 1 (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14077261000146112 Griscelli type 1 nl Synonym (core metadata concept) Active Entire term case sensitive (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
Hypopigmentation-immunodeficiency disease type 1 (disorder) Is a Hypopigmentation-immunodeficiency disease true Inferred relationship Some
Hypopigmentation-immunodeficiency disease type 1 (disorder) Occurrence Congenital true Inferred relationship Some 1
Hypopigmentation-immunodeficiency disease type 1 (disorder) Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Hypopigmentation-immunodeficiency disease type 1 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Hypopigmentation-immunodeficiency disease type 1 (disorder) Occurrence Congenital true Inferred relationship Some 2
Hypopigmentation-immunodeficiency disease type 1 (disorder) Finding site Structure of immune system (body structure) true Inferred relationship Some 2
Hypopigmentation-immunodeficiency disease type 1 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Hypopigmentation-immunodeficiency disease type 1 (disorder) Occurrence Congenital true Inferred relationship Some 3
Hypopigmentation-immunodeficiency disease type 1 (disorder) Finding site Structure of immune system (body structure) true Inferred relationship Some 3
Hypopigmentation-immunodeficiency disease type 1 (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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