723443003: Neutrophil immunodeficiency syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome

\White blood cell disorder\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\White blood cell disorder\Qualitative abnormality of granulocyte\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\White blood cell disorder\Disorder of neutrophils\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of immune function\Hereditary disorder of immune system\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Immunodeficiency associated with chromosomal abnormality\Neutrophil immunodeficiency syndrome
\Disease\Disorder of immune function\White blood cell disorder\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of immune function\White blood cell disorder\Qualitative abnormality of granulocyte\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of immune function\White blood cell disorder\Disorder of neutrophils\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of cellular component of blood\White blood cell disorder\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of cellular component of blood\White blood cell disorder\Qualitative abnormality of granulocyte\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of cellular component of blood\White blood cell disorder\Disorder of neutrophils\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder\Heritable disorder of neutrophil function\Neutrophil immunodeficiency syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3424634010 Neutrophil immunodeficiency syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3424635011 Neutrophil immunodeficiency syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Neutrophil immunodeficiency syndrome	Due to	Chromosomal disorder	true	Inferred relationship	Existential restriction modifier	1
Neutrophil immunodeficiency syndrome	Is a	Immunodeficiency associated with chromosomal abnormality	true	Inferred relationship	Existential restriction modifier
Neutrophil immunodeficiency syndrome	Is a	Heritable disorder of neutrophil function	true	Inferred relationship	Existential restriction modifier
Neutrophil immunodeficiency syndrome	Finding site	Body system structure	true	Inferred relationship	Existential restriction modifier	3
Neutrophil immunodeficiency syndrome	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier
Neutrophil immunodeficiency syndrome	Pathological process	Abnormal immune process	true	Inferred relationship	Existential restriction modifier	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
3424634010	Neutrophil immunodeficiency syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3424635011	Neutrophil immunodeficiency syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module