9434008: Hereditary pyropoikilocytosis (disorder)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\anémie\anémie causée par une anomalie constitutionnelle des érythrocytes\Hereditary pyropoikilocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Erythrocyte membrane abnormality\Hereditary pyropoikilocytosis
\Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary pyropoikilocytosis
\Disease\affection d'un système corporel\anomalie de la lignée rouge\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	est défini par la manifestation de (attribut)	Erythropenia	false	Inferred relationship	Some
Hereditary pyropoikilocytosis	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Hereditary pyropoikilocytosis	est un(e) (attribut)	Hereditary red blood cell disorder (disorder)	true	Inferred relationship	Some
Hereditary pyropoikilocytosis	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary pyropoikilocytosis	est un(e) (attribut)	anémie causée par une anomalie constitutionnelle des érythrocytes	true	Inferred relationship	Some
Hereditary pyropoikilocytosis	est un(e) (attribut)	Erythrocyte membrane abnormality	true	Inferred relationship	Some
Hereditary pyropoikilocytosis	a pour interprétation (attribut)	au-dessous de l'étendue de référence	false	Inferred relationship	Some	1
Hereditary pyropoikilocytosis	interprète (attribut)	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
Hereditary pyropoikilocytosis	a pour interprétation (attribut)	au-dessous de l'étendue de référence	false	Inferred relationship	Some	2
Hereditary pyropoikilocytosis	interprète (attribut)	Red blood cell count	false	Inferred relationship	Some	2
Hereditary pyropoikilocytosis	localisation d'une constatation (attribut)	Erythrocyte	true	Inferred relationship	Some	3
Hereditary pyropoikilocytosis	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1235831017	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	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
392061000241115	pyropoïkilocytose héréditaire (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
838264013	Hereditary pyropoikilocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
970411000172117	pyropoïkilocytose héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)