127040003: Sickle cell-hemoglobin SS disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Finding of substance level\Protein level - finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Sickle cell-haemoglobin SS disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Sickle cell-haemoglobin SS disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Sickle cell-haemoglobin SS disease
\Evaluation finding\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Sickle cell-haemoglobin SS disease
\Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Sickle cell-haemoglobin SS disease

\Finding of blood, lymphatics and immune system\Blood disease\...

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\...

\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease

\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease

\Anaemia\Anaemia due to substance\Sickle cell-haemoglobin SS disease
\Anaemia\Anaemia due to intrinsic red cell abnormality\Sickle cell-haemoglobin SS disease
\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Sickle cell-haemoglobin SS disease

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Anaemia\Anaemia due to substance\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Anaemia\Anaemia due to intrinsic red cell abnormality\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease
\Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-haemoglobin SS disease
\Disease\Congenital disease\Hereditary haemoglobinopathy\Homozygous hemoglobinopathy\Sickle cell-haemoglobin SS disease

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

206337013 Hemoglobin S-S disease en Synonym Active Initial character case insensitive SNOMED CT core

206338015 Drepanocythemia en Synonym Active Case insensitive SNOMED CT core

2547671019 Hb SS disease en Synonym Active Case sensitive SNOMED CT core

2663794019 Hereditary hemoglobinopathy disorder homozygous for hemoglobin S en Synonym Active Initial character case insensitive SNOMED CT core

328014 Sickle cell anemia en Synonym Active Case insensitive SNOMED CT core

3688057012 Sickle cell-hemoglobin SS disease en Synonym Active Initial character case insensitive SNOMED CT core

3688058019 Sickle cell-haemoglobin SS disease en Synonym Active Initial character case insensitive SNOMED CT core

3688059010 Sickle cell-hemoglobin SS disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

3780079019 Hereditary haemoglobinopathy disorder homozygous for haemoglobin S en Synonym Active Initial character case insensitive SNOMED CT core

474021015 Drepanocythaemia en Synonym Active Case insensitive SNOMED CT core

474022010 Sickle cell anaemia en Synonym Active Case insensitive SNOMED CT core

474023017 Haemoglobin S disease en Synonym Active Initial character case insensitive SNOMED CT core

474024011 Haemoglobin S-S disease en Synonym Active Initial character case insensitive SNOMED CT core

474025012 Hemoglobin S disease en Synonym Active Initial character case insensitive SNOMED CT core

474026013 Hb S disease en Synonym Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sickle cell-haemoglobin SS disease	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	1
Sickle cell-haemoglobin SS disease	Is a	Haemoglobinopathy	false	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Is a	Anaemia	false	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Is a	Anaemia due to disturbance of haemoglobin synthesis	true	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Is a	Anaemia due to intrinsic red cell abnormality	true	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some	1
Sickle cell-haemoglobin SS disease	Is a	Drug-related disorder	false	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Is a	Disorder by body site	false	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Finding site	Erythroid cell	false	Inferred relationship	Some	1
Sickle cell-haemoglobin SS disease	Is a	Sickling disorder due to haemoglobin S	true	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Is a	Homozygous hemoglobinopathy	true	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Finding site	Body system structure	false	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Is a	Anaemia due to substance	true	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Has interpretation	Below reference range	true	Inferred relationship	Some	1
Sickle cell-haemoglobin SS disease	Has interpretation	Below reference range	false	Inferred relationship	Some	2
Sickle cell-haemoglobin SS disease	Interprets	Red blood cell count	false	Inferred relationship	Some	1
Sickle cell-haemoglobin SS disease	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	2
Sickle cell-haemoglobin SS disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Causative agent	Haemoglobin S	true	Inferred relationship	Some	5
Sickle cell-haemoglobin SS disease	Associated morphology	Drepanocyte	true	Inferred relationship	Some	4
Sickle cell-haemoglobin SS disease	Finding site	Erythrocyte	false	Inferred relationship	Some
Sickle cell-haemoglobin SS disease	Finding site	Entire haematological system	false	Inferred relationship	Some	1
Sickle cell-haemoglobin SS disease	Occurrence	Congenital	true	Inferred relationship	Some	3
Sickle cell-haemoglobin SS disease	Finding site	Erythrocyte	true	Inferred relationship	Some	3
Sickle cell-haemoglobin SS disease	Is a	Congenital anaemia	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acute chest syndrome due to sickle cell thalassaemia with crisis	Following	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	2
Acute chest syndrome due to sickle cell haemoglobin C disease with crisis	Following	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	2
Sickle cell-haemoglobin Lepore disease	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell-Haemoglobin O Arab disease	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell nephropathy	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Hand-foot syndrome in sickle cell anaemia	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Haemoglobin S disease without crisis	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell-haemoglobin D disease	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell-haemoglobin C disease	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell-thalassaemia disease	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell-haemoglobin E disease	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
FH: Sickle cell anaemia	Associated finding	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	1
Acute chest syndrome	Following	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	1
Haemoglobin S disease with crisis	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell anaemia with crisis	Is a	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Haemoglobin SS disease without crisis	Is a	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell anaemia with coexistent alpha-thalassaemia	Is a	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell-haemoglobin C retinopathy	Due to	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	3
Sickle cell retinopathy	Due to	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	2
Proliferative retinopathy due to sickle cell disease	Due to	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	2
Sickle cell anaemia with no crisis	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell anaemia with crisis	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Antenatal sickle cell screening	Has focus	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	1
FH: Sickle cell anaemia	Associated finding	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	1
Screening for sickle cell disease	Has focus	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	2
Antenatal sickle cell screening	Has focus	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	2
H/O: sickle cell anaemia	Associated finding	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	1
H/O: sickle cell anaemia	Associated finding	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	1
FH: Sickle cell anaemia	Associated finding	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some	1
Sickle cell anaemia of unspecified type	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell anaemia NOS	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
[X]Other sickle cell disorders	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell anaemia with high haemoglobin F	Is a	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell anaemia in mother complicating childbirth	Is a	True	Sickle cell-haemoglobin SS disease	Inferred relationship	Some
Sickle cell retinopathy	Is a	False	Sickle cell-haemoglobin SS disease	Inferred relationship	Some

Reference Sets

Emergency department reference set

Australian emergency department reference set

NSW Emergency Department reference set

Clinical finding foundation reference set

Emergency department diagnosis reference set

Problem/Diagnosis reference set

Back to Start

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