9434008: Hereditary pyropoikilocytosis (disorder)

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

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

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis

\Anaemia\Anaemia due to intrinsic red cell abnormality\Hereditary pyropoikilocytosis

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary pyropoikilocytosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to intrinsic red cell abnormality\Hereditary pyropoikilocytosis
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary pyropoikilocytosis
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\Disorder of body system\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary pyropoikilocytosis

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
Hereditary pyropoikilocytosis	Is a	Anaemia due to intrinsic red cell abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis	Is a	Erythrocyte membrane abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary pyropoikilocytosis	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis	Has definitional manifestation	érythropénie	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis	Is a	Hereditary red blood cell disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary pyropoikilocytosis	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary pyropoikilocytosis	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary pyropoikilocytosis	Interprets	Red blood cell count	false	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

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Id	Description	Lang	Type	Status	Case?	Module
16531015	Hereditary pyropoikilocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
838264013	Hereditary pyropoikilocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5244177018	HPP - hereditary pyropoikilocytosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
16531015	Hereditary pyropoikilocytosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
16531015	Hereditary pyropoikilocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
16532010	HPP	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
838264013	Hereditary pyropoikilocytosis (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
838264013	Hereditary pyropoikilocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1235831017	HPP - Hereditary pyropoikilocytosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1235831017	HPP - Hereditary pyropoikilocytosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5244177018	HPP - hereditary pyropoikilocytosis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
970411000172117	pyropoïkilocytose héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
970411000172117	pyropoïkilocytose héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module