16964007: Hereditary persistence of fetal hemoglobin thalassemia (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\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Evaluation finding\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia

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

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia
\Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia

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

Descriptions:

Id Description Lang Type Status Case? Module

2793345010 Hereditary persistence of foetal haemoglobin thalassaemia en Synonym Active Case insensitive SNOMED CT core

28713012 Hereditary persistence of fetal hemoglobin thalassemia en Synonym Active Case insensitive SNOMED CT core

28716016 HPFH en Synonym Active Case sensitive SNOMED CT core

478010018 Hereditary persistence of fetal haemoglobin thalassaemia en Synonym Active Case insensitive SNOMED CT core

744092016 Hereditary persistence of fetal hemoglobin thalassemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary persistence of fetal haemoglobin thalassaemia	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
Hereditary persistence of fetal haemoglobin thalassaemia	Is a	Thalassaemia	true	Inferred relationship	Some
Hereditary persistence of fetal haemoglobin thalassaemia	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Hereditary persistence of fetal haemoglobin thalassaemia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Hereditary persistence of fetal haemoglobin thalassaemia	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary persistence of fetal haemoglobin thalassaemia	Has interpretation	Below reference range	false	Inferred relationship	Some	1
Hereditary persistence of fetal haemoglobin thalassaemia	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
Hereditary persistence of fetal haemoglobin thalassaemia	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Hereditary persistence of fetal haemoglobin thalassaemia	Interprets	Red blood cell count	false	Inferred relationship	Some	2
Hereditary persistence of fetal haemoglobin thalassaemia	Occurrence	Congenital	true	Inferred relationship	Some	3
Hereditary persistence of fetal haemoglobin thalassaemia	Finding site	Erythrocyte	true	Inferred relationship	Some	3
Hereditary persistence of fetal haemoglobin thalassaemia	Finding site	Erythrocyte	false	Inferred relationship	Some
Hereditary persistence of fetal haemoglobin thalassaemia	Finding site	Haematopoietic system structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary persistence of fetal haemoglobin unlinked to beta-globulin gene cluster	Is a	True	Hereditary persistence of fetal haemoglobin thalassaemia	Inferred relationship	Some
HPFH A gamma beta^+^ thalassaemia	Is a	True	Hereditary persistence of fetal haemoglobin thalassaemia	Inferred relationship	Some
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia	Is a	True	Hereditary persistence of fetal haemoglobin thalassaemia	Inferred relationship	Some
HPFH nondeletion type	Is a	True	Hereditary persistence of fetal haemoglobin thalassaemia	Inferred relationship	Some
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia	Is a	True	Hereditary persistence of fetal haemoglobin thalassaemia	Inferred relationship	Some
Hereditary persistence of fetal haemoglobin deletion type	Is a	True	Hereditary persistence of fetal haemoglobin thalassaemia	Inferred relationship	Some
HPFH linked to beta-globulin gene cluster	Is a	True	Hereditary persistence of fetal haemoglobin thalassaemia	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

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