FHIR © HL7.org | Server Home | FHIR Server FHIR Server 4.0.1 | FHIR Version n/a User: [n/a]

1254947002: Hypopigmentation-immunodeficiency disease type 3 (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Disorder of pigmentation\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 3

\Disorder of immune function\Immunodeficiency disorder\...

\Primary immune deficiency disorder\Immunodeficiency with major anomalies\Immunodeficiency associated with multiple organ system abnormalities\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 3

\Congenital immunodeficiency disease\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 3

\Disorder of body system\Disorder of immune structure\Immunodeficiency with major anomalies\Immunodeficiency associated with multiple organ system abnormalities\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 3

\Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 3

\Congenital disease\Congenital malformation\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 3
\Congenital disease\Congenital immunodeficiency disease\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 3

\Developmental disorder\Congenital malformation\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 3

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

Descriptions:

Id Description Lang Type Status Case? Module

5143924016 Hypopigmentation-immunodeficiency disease type 3 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5143925015 Griscelli syndrome type 3 en Synonym Active Entire term case sensitive SNOMED CT core module
5146508015 Hypopigmentation-immunodeficiency disease type 3 en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hypopigmentation-immunodeficiency disease type 3	Is a	Hypopigmentation-immunodeficiency disease	true	Inferred relationship	Existential restriction modifier
Hypopigmentation-immunodeficiency disease type 3	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Hypopigmentation-immunodeficiency disease type 3	Associated morphology	Decreased melanin pigmentation	true	Inferred relationship	Existential restriction modifier	1
Hypopigmentation-immunodeficiency disease type 3	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Hypopigmentation-immunodeficiency disease type 3	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Hypopigmentation-immunodeficiency disease type 3	Finding site	Structure of immune system	true	Inferred relationship	Existential restriction modifier	2
Hypopigmentation-immunodeficiency disease type 3	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Hypopigmentation-immunodeficiency disease type 3	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Hypopigmentation-immunodeficiency disease type 3	Finding site	Structure of immune system	true	Inferred relationship	Existential restriction modifier	3
Hypopigmentation-immunodeficiency disease type 3	Pathological process	Abnormal immune process	true	Inferred relationship	Existential restriction modifier	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
5143924016	Hypopigmentation-immunodeficiency disease type 3 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
5143925015	Griscelli syndrome type 3	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
5146508015	Hypopigmentation-immunodeficiency disease type 3	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module