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61777009: Thalassemia-hemoglobin C disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\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 (disorder)\Hereditary hemoglobinopathy (disorder)\...

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

\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease

\Procedure related finding\Evaluation finding\...

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin 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 (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Haemoglobin C disease\Thalassemia-hemoglobin C disease
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Thalassemia-hemoglobin C disease

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Thalassemia-hemoglobin C disease	Is a	Haemoglobin C disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease	Is a	Thalassemia with other hemoglobinopathy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease	Has definitional manifestation	érythropénie	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Thalassemia-hemoglobin C disease	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Thalassemia-hemoglobin C disease	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Thalassemia-hemoglobin C disease	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Thalassemia-hemoglobin C disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Thalassemia-hemoglobin C disease	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Thalassemia-hemoglobin C disease	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Existential restriction modifier (core metadata concept)	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 (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
102667010	Thalassemia-hemoglobin C disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499117018	Haemoglobin C-F disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499118011	Thalassaemia-haemoglobin C disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
800876015	Thalassemia-hemoglobin C disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
102666018	Hemoglobin C-F disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
102667010	Thalassemia-hemoglobin C disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499117018	Haemoglobin C-F disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
499118011	Thalassaemia-haemoglobin C disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
800876015	Thalassemia-hemoglobin C disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3444351001000112	Hämoglobin C - Beta-Thalassämie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3444351001000112	Hämoglobin C - Beta-Thalassämie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module