1187119002: Hereditary pediatric Behçet-like disease (disorder)

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

\Genetic disease\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary paediatric Behçet-like disease
\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary paediatric Behçet-like disease

\Disorder of immune function (disorder)\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
\Disorder of immune function (disorder)\Hereditary disorder of immune system\Hereditary paediatric Behçet-like disease

\Disorder of body system\Disorder of immune structure (disorder)\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary paediatric Behçet-like disease

\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease

\Recurrent disease\Hereditary paediatric Behçet-like disease

\Systemic disease\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease

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

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