5300004: Hemoglobin Bart's hydrops syndrome (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\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\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\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Red blood cell count outside reference range\Red blood cell count below reference range\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Cytopenia\Red blood cell count below reference range\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Hemoglobin below reference range\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\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\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\Red blood cell count below reference range\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\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\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Measurement finding\Finding of red blood cell count\Red blood cell count outside reference range\Red blood cell count below reference range\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Hematopoietic system finding\Hematology test outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\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\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome

\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\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome

\Anemia\Fetal anemia\Hemoglobin Bart's hydrops syndrome
\Anemia\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome

\Edema\Disorder characterized by edema\Hydrops fetalis\Hemoglobin Bart's hydrops syndrome

\Fetal finding\Fetal disorder\...

\Fetal anemia\Hemoglobin Bart's hydrops syndrome

\Hydrops fetalis\Hemoglobin Bart's hydrops syndrome

\Fetus with hereditary disease\Hemoglobin Bart's hydrops syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Genetic disease\Hereditary disease\Fetus with hereditary disease\Hemoglobin Bart's hydrops syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of fetus or newborn\Fetal disorder\Fetal anemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of fetus or newborn\Fetal disorder\Hydrops fetalis\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of fetus or newborn\Fetal disorder\Fetus with hereditary disease\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of cellular component of blood\Anemia\Fetal anemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of cellular component of blood\Anemia\Congenital anemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Disorder characterized by edema\Hydrops fetalis\Hemoglobin Bart's hydrops syndrome
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Alpha thalassemia\Hemoglobin Bart's hydrops syndrome
\Disease\Congenital disease\Congenital anemia\Hemoglobin Bart's hydrops syndrome

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
Hemoglobin Bart's hydrops syndrome	Is a	Alpha thalassemia	true	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier	1
Hemoglobin Bart's hydrops syndrome	Associated morphology	Hydrops	false	Inferred relationship	Existential restriction modifier	1
Hemoglobin Bart's hydrops syndrome	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	1
Hemoglobin Bart's hydrops syndrome	Is a	Disorder by body site	false	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Finding site	Anatomical structure	false	Inferred relationship	Existential restriction modifier	1
Hemoglobin Bart's hydrops syndrome	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Finding site	Anatomical structure	false	Inferred relationship	Existential restriction modifier	1
Hemoglobin Bart's hydrops syndrome	Associated morphology	Hydrops	true	Inferred relationship	Existential restriction modifier	4
Hemoglobin Bart's hydrops syndrome	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	1
Hemoglobin Bart's hydrops syndrome	Interprets	Red blood cell count	true	Inferred relationship	Existential restriction modifier	1
Hemoglobin Bart's hydrops syndrome	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Hemoglobin Bart's hydrops syndrome	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	2
Hemoglobin Bart's hydrops syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Hemoglobin Bart's hydrops syndrome	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Hemoglobin Bart's hydrops syndrome	Is a	Disorder characterized by edema	false	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Is a	Hydrops fetalis	true	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Is a	Fetal anemia	true	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Occurrence	Fetal period	true	Inferred relationship	Existential restriction modifier	4
Hemoglobin Bart's hydrops syndrome	Is a	Congenital anemia	true	Inferred relationship	Existential restriction modifier
Hemoglobin Bart's hydrops syndrome	Is a	Fetus with hereditary disease	true	Inferred relationship	Existential restriction modifier

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
9888011	Hemoglobin Bart's hydrops syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
9889015	Hemoglobin Bart's disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
496516017	Alpha thalassemia major	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
496517014	Hemoglobin Barts hydrops	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
496518016	Haemoglobin Bart's hydrops syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
496519012	Alpha thalassaemia major	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
496520018	Haemoglobin Bart's disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
496521019	Haemoglobin Barts hydrops	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
791071016	Hemoglobin Bart's hydrops syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
2841557010	Haemoglobin Bart hydrops syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2841558017	Hemoglobin Bart hydrops syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2800971000000113	Homozygous alpha zero thalassaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT United Kingdom Edition module
2800981000000110	Hb (haemoglobin) Bart's hydrops fetalis	en	Synonym	Active	Entire term case sensitive	SNOMED CT United Kingdom Edition module