61777009: Thalassemia-hemoglobin C disease (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\Thalassemia-hemoglobin C disease
\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\Thalassemia-hemoglobin C disease
\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\Thalassemia-hemoglobin C disease
\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\Thalassemia-hemoglobin C disease
\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\Thalassemia-hemoglobin C disease

\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\...

\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease\Thalassemia-hemoglobin C disease

\Thalassemia\Thalassemia with other hemoglobinopathy\Thalassemia-hemoglobin C disease

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

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease\Thalassemia-hemoglobin C disease
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Thalassemia-hemoglobin C disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease\Thalassemia-hemoglobin C disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Thalassemia-hemoglobin C disease

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

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

102666018 Hemoglobin C-F disease en Synonym Active Entire term case sensitive SNOMED CT core module

102667010 Thalassemia-hemoglobin C disease en Synonym Active Only initial character case insensitive SNOMED CT core module

499117018 Haemoglobin C-F disease en Synonym Active Only initial character case insensitive SNOMED CT core module

499118011 Thalassaemia-haemoglobin C disease en Synonym Active Only initial character case insensitive SNOMED CT core module

800876015 Thalassemia-hemoglobin C disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
102666018	Hemoglobin C-F disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
102667010	Thalassemia-hemoglobin C disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
499117018	Haemoglobin C-F disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
499118011	Thalassaemia-haemoglobin C disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
800876015	Thalassemia-hemoglobin C disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module