47047009: Thalassemia with other hemoglobinopathy (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\Thalassemia with other hemoglobinopathy
\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\Thalassemia with other hemoglobinopathy
\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\Thalassemia with other hemoglobinopathy
\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\Thalassemia with other hemoglobinopathy
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia with other hemoglobinopathy

\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\Thalassemia with other hemoglobinopathy

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia with other hemoglobinopathy

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy

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

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

78417011 Thalassemia with other hemoglobinopathy en Synonym Active Entire term case insensitive SNOMED CT core module

494734018 Thalassaemia with other haemoglobinopathy en Synonym Active Entire term case insensitive SNOMED CT core module

784462017 Thalassemia with other hemoglobinopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-thalassemia disease	Is a	True	Thalassemia with other hemoglobinopathy	Inferred relationship	Existential restriction modifier
Thalassemia-hemoglobin C disease	Is a	True	Thalassemia with other hemoglobinopathy	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
78417011	Thalassemia with other hemoglobinopathy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
494734018	Thalassaemia with other haemoglobinopathy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
784462017	Thalassemia with other hemoglobinopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module