40145002: Congenital neutrophil actin dysfunction (disorder)

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

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\White blood cell disorder\...

\Qualitative abnormality of granulocyte\Congenital neutrophil actin dysfunction

\Disorder of neutrophils\Congenital neutrophil actin dysfunction

\Disease\Disorder of immune function (disorder)\White blood cell disorder\Qualitative abnormality of granulocyte\Congenital neutrophil actin dysfunction
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Disorder of neutrophils\Congenital neutrophil actin dysfunction
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital neutrophil actin dysfunction
\Disease\Disorder of cellular component of blood\White blood cell disorder\Qualitative abnormality of granulocyte\Congenital neutrophil actin dysfunction
\Disease\Disorder of cellular component of blood\White blood cell disorder\Disorder of neutrophils\Congenital neutrophil actin dysfunction

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital neutrophil actin dysfunction	Is a	Disorder of neutrophils	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Is a	Qualitative abnormality of granulocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Finding site	Leucocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Finding site	Structure of immune system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Associated morphology	White blood cell abnormality (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Is a	Congenital anomaly of the haematopoietic system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital neutrophil actin dysfunction	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Has definitional manifestation	White blood cell finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital neutrophil actin dysfunction	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

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
63729015	Congenital neutrophil actin dysfunction	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
63730013	Actin dysfunction syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
776732016	Congenital neutrophil actin dysfunction (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
63729015	Congenital neutrophil actin dysfunction	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
63729015	Congenital neutrophil actin dysfunction	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
63730013	Actin dysfunction syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
63730013	Actin dysfunction syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
776732016	Congenital neutrophil actin dysfunction (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
776732016	Congenital neutrophil actin dysfunction (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
123011000077114	anomalie congénitale de l'actine des neutrophiles	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
123011000077114	anomalie congénitale de l'actine des neutrophiles	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module