402794002: Heritable disorder of neutrophil function (disorder)

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

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

\Hereditary disorder of cellular element of blood (disorder)\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)

\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)
\White blood cell disorder\Qualitative abnormality of granulocyte\Heritable disorder of neutrophil function (disorder)
\White blood cell disorder\Disorder of neutrophils\Disorder of neutrophil function\Heritable disorder of neutrophil function (disorder)
\White blood cell disorder\Disorder of neutrophils\Heritable disorder of neutrophil function (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of immune function (disorder)\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Qualitative abnormality of granulocyte\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Disorder of neutrophils\Disorder of neutrophil function\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of immune function (disorder)\White blood cell disorder\Disorder of neutrophils\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of cellular component of blood (disorder)\White blood cell disorder\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of cellular component of blood (disorder)\White blood cell disorder\Qualitative abnormality of granulocyte\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of cellular component of blood (disorder)\White blood cell disorder\Disorder of neutrophils\Disorder of neutrophil function\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of cellular component of blood (disorder)\White blood cell disorder\Disorder of neutrophils\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary white blood cell disorder (disorder)\Heritable disorder of neutrophil function (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1770718019 Heritable disorder of neutrophil function (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1781886016 Heritable disorder of neutrophil function en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

374571000052115 ärftlig störning av neutrofilfunktion sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Heritable disorder of neutrophil function (disorder)	Is a	Disorder of neutrophils	true	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Finding site	Leukocyte	false	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Finding site	Structure of immune system (body structure)	false	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Associated morphology	White blood cell abnormality (morphologic abnormality)	false	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Has definitional manifestation	White blood cell finding	false	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Is a	Hereditary white blood cell disorder (disorder)	true	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Is a	Qualitative abnormality of granulocyte	true	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Finding site	Body system structure	true	Inferred relationship	Some	1
Heritable disorder of neutrophil function (disorder)	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
Heritable disorder of neutrophil function (disorder)	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	2
Heritable disorder of neutrophil function (disorder)	Is a	Disorder of neutrophil function	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Jung syndrome (disorder)	Is a	True	Heritable disorder of neutrophil function (disorder)	Inferred relationship	Some
Siccardi syndrome (disorder)	Is a	True	Heritable disorder of neutrophil function (disorder)	Inferred relationship	Some
Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome (disorder)	Is a	True	Heritable disorder of neutrophil function (disorder)	Inferred relationship	Some
Neutrophil immunodeficiency syndrome (disorder)	Is a	True	Heritable disorder of neutrophil function (disorder)	Inferred relationship	Some
Susceptibility to localized juvenile periodontitis	Is a	True	Heritable disorder of neutrophil function (disorder)	Inferred relationship	Some

Reference Sets

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1770718019	Heritable disorder of neutrophil function (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1781886016	Heritable disorder of neutrophil function	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
374571000052115	ärftlig störning av neutrofilfunktion	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)