16964007: Hereditary persistence of fetal hemoglobin thalassemia (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\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\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\Hereditary persistence of fetal hemoglobin thalassemia
\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\Hereditary persistence of fetal hemoglobin thalassemia
\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\Hereditary persistence of fetal hemoglobin thalassemia
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia

\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\Hereditary persistence of fetal hemoglobin thalassemia

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia

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

Descriptions:

Id Description Lang Type Status Case? Module

28713012 Hereditary persistence of fetal hemoglobin thalassemia en Synonym Active Entire term case insensitive SNOMED CT core module

28716016 HPFH en Synonym Active Entire term case sensitive SNOMED CT core module

478010018 Hereditary persistence of fetal haemoglobin thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module

744092016 Hereditary persistence of fetal hemoglobin thalassemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2793345010 Hereditary persistence of foetal haemoglobin thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary persistence of fetal hemoglobin thalassemia	Is a	Thalassemia	true	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin thalassemia	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin thalassemia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin thalassemia	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin thalassemia	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Hereditary persistence of fetal hemoglobin thalassemia	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Hereditary persistence of fetal hemoglobin thalassemia	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Hereditary persistence of fetal hemoglobin thalassemia	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	2
Hereditary persistence of fetal hemoglobin thalassemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Hereditary persistence of fetal hemoglobin thalassemia	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Hereditary persistence of fetal hemoglobin thalassemia	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster	Is a	True	Hereditary persistence of fetal hemoglobin thalassemia	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia	Is a	True	Hereditary persistence of fetal hemoglobin thalassemia	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia	Is a	True	Hereditary persistence of fetal hemoglobin thalassemia	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin, nondeletion type	Is a	True	Hereditary persistence of fetal hemoglobin thalassemia	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia	Is a	True	Hereditary persistence of fetal hemoglobin thalassemia	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin deletion type	Is a	True	Hereditary persistence of fetal hemoglobin thalassemia	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster	Is a	True	Hereditary persistence of fetal hemoglobin thalassemia	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
28713012	Hereditary persistence of fetal hemoglobin thalassemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
28716016	HPFH	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
478010018	Hereditary persistence of fetal haemoglobin thalassaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
744092016	Hereditary persistence of fetal hemoglobin thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
2793345010	Hereditary persistence of foetal haemoglobin thalassaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module