127040003: Sickle cell-hemoglobin SS disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Finding of substance level\Finding of protein level\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\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\Hemoglobin below reference range\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\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease
\Evaluation finding\Hematopoietic system finding\Hematology test outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease

\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\Hereditary hemoglobinopathy\...

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

\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease

\Anemia\Anemia caused by substance\Sickle cell-hemoglobin SS disease
\Anemia\Anemia due to intrinsic red cell abnormality\Sickle cell-hemoglobin SS disease
\Anemia\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Anemia\Anemia caused by substance\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to intrinsic red cell abnormality\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-hemoglobin SS disease
\Disease\Congenital disease\Hereditary hemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-hemoglobin SS disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sickle cell-hemoglobin SS disease	Is a	Hemoglobinopathy	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Is a	Anemia	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Causative agent	Hemoglobin S	true	Inferred relationship	Existential restriction modifier	5
Sickle cell-hemoglobin SS disease	Associated morphology	Drepanocyte	true	Inferred relationship	Existential restriction modifier	4
Sickle cell-hemoglobin SS disease	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin SS disease	Is a	Anemia due to disturbance of hemoglobin synthesis	true	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Is a	Anemia due to intrinsic red cell abnormality	true	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin SS disease	Is a	Drug-related disorder	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Is a	Disorder by body site	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Finding site	Erythroid cell	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin SS disease	Is a	Sickling disorder due to hemoglobin S	true	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Is a	Homozygous hemoglobinopathy	true	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Is a	Anemia caused by substance	true	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin SS disease	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-hemoglobin SS disease	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin SS disease	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-hemoglobin SS disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Sickle cell-hemoglobin SS disease	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Sickle cell-hemoglobin SS disease	Is a	Congenital anemia	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell anemia with high hemoglobin F	Is a	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell retinopathy	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin Lepore disease	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Hemoglobin S disease without crisis	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin D disease	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin E disease	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Hemoglobin S disease with crisis	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell anemia with no crisis	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell anemia with crisis	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell anemia of unspecified type	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell anemia NOS	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
[X]Other sickle cell disorders	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell nephropathy	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Hand-foot syndrome in sickle cell anemia	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Family history of sickle cell anemia	Associated finding	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	1
Acute chest syndrome	After	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	1
Hemoglobin SS disease with crisis	Is a	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Hemoglobin SS disease without crisis	Is a	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell anemia with coexistent alpha-thalassemia	Is a	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C retinopathy	Due to	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	3
Sickle cell retinopathy	Due to	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	2
Proliferative retinopathy due to sickle cell disease	Due to	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	2
Antenatal sickle cell screening	Has focus	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	1
Family history of sickle cell anemia	Associated finding	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	1
Screening for sickle cell disease	Has focus	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	2
Antenatal sickle cell screening	Has focus	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	2
History of sickle cell anemia	Associated finding	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	1
History of sickle cell anemia	Associated finding	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	1
Family history of sickle cell anemia	Associated finding	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	1
Sickle cell anemia in mother complicating childbirth	Is a	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Acute chest syndrome due to sickle cell thalassemia with crisis	After	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	2
Acute chest syndrome due to sickle cell hemoglobin C disease with crisis	After	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	2
[X]Other sickle cell disorders	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with sickle cell-Haemoglobin SS disease (situation)	Associated finding	True	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier	1
Sickle cell anemia of unspecified type (disorder)	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier
Sickle cell anemia NOS (disorder)	Is a	False	Sickle cell-hemoglobin SS disease	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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