127040003: drépanocytose (trouble)

SNOMED CT Concept\constatation clinique\...

\Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease
\Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease

\constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...

\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\...

\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease

\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease

\anémie\Anaemia due to substance\Sickle cell-hemoglobin SS disease
\anémie\anémie causée par une anomalie constitutionnelle des érythrocytes\Sickle cell-hemoglobin SS disease
\anémie\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease

\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\anémie\Anaemia due to substance\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\anémie\anémie causée par une anomalie constitutionnelle des érythrocytes\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\anémie\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-hemoglobin SS disease
\Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease

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
Sickle cell-hemoglobin SS disease	interprète (attribut)	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	1
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	Hemoglobinopathy	false	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	anémie	false	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	Anemia due to disturbance of hemoglobin synthesis	true	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	anémie causée par une anomalie constitutionnelle des érythrocytes	true	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	est défini par la manifestation de (attribut)	Erythropenia	false	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some	1
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	Drug-related disorder	false	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	trouble selon la localisation corporelle	false	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	localisation d'une constatation (attribut)	Erythroid cell (cell)	false	Inferred relationship	Some	1
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	Sickling disorder due to hemoglobin S (disorder)	true	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	Homozygous hemoglobinopathy	true	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	Anaemia due to substance	true	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	a pour interprétation (attribut)	au-dessous de l'étendue de référence	true	Inferred relationship	Some	1
Sickle cell-hemoglobin SS disease	a pour interprétation (attribut)	au-dessous de l'étendue de référence	false	Inferred relationship	Some	2
Sickle cell-hemoglobin SS disease	interprète (attribut)	Red blood cell count	false	Inferred relationship	Some	1
Sickle cell-hemoglobin SS disease	interprète (attribut)	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	2
Sickle cell-hemoglobin SS disease	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	Causative agent	Haemoglobin S	true	Inferred relationship	Some	5
Sickle cell-hemoglobin SS disease	morphologie associée (attribut)	Drepanocyte (cell)	true	Inferred relationship	Some	4
Sickle cell-hemoglobin SS disease	localisation d'une constatation (attribut)	Erythrocyte	false	Inferred relationship	Some
Sickle cell-hemoglobin SS disease	localisation d'une constatation (attribut)	Entire hematological system (body structure)	false	Inferred relationship	Some	1
Sickle cell-hemoglobin SS disease	survenue (attribut)	congénital	true	Inferred relationship	Some	3
Sickle cell-hemoglobin SS disease	localisation d'une constatation (attribut)	Erythrocyte	true	Inferred relationship	Some	3
Sickle cell-hemoglobin SS disease	est un(e) (attribut)	Congenital anemia	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acute chest syndrome due to sickle cell thalassaemia with crisis	After	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	2
Acute chest syndrome due to sickle cell haemoglobin C disease with crisis	After	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	2
Sickle cell-hemoglobin Lepore disease	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell-Hemoglobin O Arab disease	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell nephropathy	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Hand-foot syndrome in sickle cell anemia (disorder)	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Hemoglobin S disease without crisis	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
drépanocytose - hémoglobinose D (trouble)	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
drépanocytose - hémoglobinose C	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell-thalassaemia disease	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell-haemoglobin E disease	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Family history of sickle cell anaemia	constatation associée (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	1
Acute chest syndrome (disorder)	After	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	1
Hemoglobin S disease with crisis	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Hemoglobin SS disease with crisis (disorder)	est un(e) (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Hemoglobin SS disease without crisis (disorder)	est un(e) (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell anemia with coexistent alpha-thalassemia	est un(e) (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell-haemoglobin C retinopathy	Due to	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	3
Sickle cell retinopathy	Due to	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	2
Proliferative retinopathy due to sickle cell disease	Due to	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	2
Sickle cell anemia with no crisis	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell anemia with crisis	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Antenatal sickle cell screening	a pour objet (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	1
Family history of sickle cell anaemia	constatation associée (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	1
Screening for sickle cell disease	a pour objet (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	2
Antenatal sickle cell screening	a pour objet (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	2
History of sickle cell anaemia	constatation associée (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	1
History of sickle cell anaemia	constatation associée (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	1
Family history of sickle cell anaemia	constatation associée (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some	1
Sickle cell anemia of unspecified type	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell anemia NOS	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
[X]Other sickle cell disorders	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell anemia with high hemoglobin F	est un(e) (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell anaemia in mother complicating childbirth	est un(e) (attribut)	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Some
Sickle cell retinopathy	est un(e) (attribut)	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Some

Reference Sets

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

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Id	Description	Lang	Type	Status	Case?	Module
206337013	Hemoglobin S-S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
206338015	Drepanocythemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2547671019	Hb SS disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2663794019	Hereditary hemoglobinopathy disorder homozygous for hemoglobin S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
328014	Sickle cell anemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3688057012	Sickle cell-hemoglobin SS disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3688058019	Sickle cell-haemoglobin SS disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3688059010	Sickle cell-hemoglobin SS disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3780079019	Hereditary haemoglobinopathy disorder homozygous for haemoglobin S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
440781000172118	drépanocytose	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
474021015	Drepanocythaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474022010	Sickle cell anaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474023017	Haemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474024011	Haemoglobin S-S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474025012	Hemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474026013	Hb S disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
517391000241112	drépanocytose (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)