414395005: Hereditary white blood cell disorder (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...

\troubles héréditaires des éléments figurés du sang\Hereditary white blood cell disorder (disorder)

\anomalie de la lignée blanche\Hereditary white blood cell disorder (disorder)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary white blood cell disorder (disorder)
\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)
\Disease\trouble de la fonction immunitaire\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)
\Disease\trouble de la fonction immunitaire\anomalie de la lignée blanche\Hereditary white blood cell disorder (disorder)
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary white blood cell disorder (disorder)
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée blanche\Hereditary white blood cell disorder (disorder)
\Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary white blood cell disorder (disorder)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2530856015 Hereditary white blood cell disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2534321015 Hereditary white blood cell disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary white blood cell disorder (disorder)	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	2
Hereditary white blood cell disorder (disorder)	est un(e) (attribut)	troubles héréditaires des éléments figurés du sang	true	Inferred relationship	Some
Hereditary white blood cell disorder (disorder)	est un(e) (attribut)	anomalie de la lignée blanche	true	Inferred relationship	Some
Hereditary white blood cell disorder (disorder)	est un(e) (attribut)	Hereditary disorder of immune system	true	Inferred relationship	Some
Hereditary white blood cell disorder (disorder)	morphologie associée (attribut)	White blood cell abnormality	false	Inferred relationship	Some
Hereditary white blood cell disorder (disorder)	est défini par la manifestation de (attribut)	constatation à propos des leucocytes	false	Inferred relationship	Some
Hereditary white blood cell disorder (disorder)	localisation d'une constatation (attribut)	structure d'un système corporel	true	Inferred relationship	Some	1
Hereditary white blood cell disorder (disorder)	est défini par la manifestation de (attribut)	Immune system finding	false	Inferred relationship	Some
Hereditary white blood cell disorder (disorder)	est défini par la manifestation de (attribut)	Immune system finding	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Poikiloderma with neutropenia	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Pancytopenia with developmental delay syndrome	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Hereditary isolated aplastic anemia	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
neutrophilie héréditaire	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
lymphohistiocytose familiale	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Onycho-tricho-dysplasia neutropenia syndrome	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Combined immunodeficiency, enteropathy spectrum	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Periodic fever, infantile enterocolitis, autoinflammatory syndrome	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
May Hegglin syndrome	est un(e) (attribut)	False	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Severe combined immunodeficiency with reticular dysgenesis (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Hereditary eosinophilia	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Chronic granulomatous disease (disorder)	est un(e) (attribut)	False	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Hereditary hypersegmentation	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Chédiak-Higashi syndrome	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Reticular dysgenesis	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Heritable disorder of neutrophil production (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
anémie de Fanconi (trouble)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Shwachman syndrome	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Periodontitis co-occurrent with infantile genetic agranulocytosis (disorder)	est un(e) (attribut)	False	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Revesz syndrome (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
WT limb blood syndrome (disorder)	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some
Ataxia pancytopenia syndrome	est un(e) (attribut)	True	Hereditary white blood cell disorder (disorder)	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2530856015	Hereditary white blood cell disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2534321015	Hereditary white blood cell disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core