86242003: Alpha plus thalassemia deletion type (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)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type

\Anaemia\Congenital anemia\Alpha plus thalassemia deletion type
\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type

\Procedure related finding\Evaluation finding\...

\Measurement finding\Finding of substance level (finding)\Finding of protein level (finding)\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Congenital anemia\Alpha plus thalassemia deletion type
\Measurement finding\Finding of substance level (finding)\Finding of protein level (finding)\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Red blood cell count outside reference range\Red blood cell count below reference range\Congenital anemia\Alpha plus thalassemia deletion type
\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Cytopenia\Red blood cell count below reference range\Congenital anemia\Alpha plus thalassemia deletion type
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin below reference range (finding)\Congenital anemia\Alpha plus thalassemia deletion type
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Cytopenia\Red blood cell count below reference range\Congenital anemia\Alpha plus thalassemia deletion type
\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Congenital anemia\Alpha plus thalassemia deletion type
\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\Red blood cell count below reference range\Congenital anemia\Alpha plus thalassemia deletion type

\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Congenital anemia\Alpha plus thalassemia deletion type
\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Congenital anemia\Alpha plus thalassemia deletion type
\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type

\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\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital anemia\Alpha plus thalassemia deletion type
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Disease\Disorder of cellular component of blood\Anaemia\Congenital anemia\Alpha plus thalassemia deletion type
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\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\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Alpha plus thalassemia\Alpha plus thalassemia deletion type

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
Alpha plus thalassemia deletion type	Is a	Alpha plus thalassemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha plus thalassemia deletion type	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha plus thalassemia deletion type	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha plus thalassemia deletion type	Has definitional manifestation	érythropénie	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha plus thalassemia deletion type	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha plus thalassemia deletion type	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha plus thalassemia deletion type	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Alpha plus thalassemia deletion type	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Alpha plus thalassemia deletion type	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Alpha plus thalassemia deletion type	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Alpha plus thalassemia deletion type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Alpha plus thalassemia deletion type	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Alpha plus thalassemia deletion type	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Alpha plus thalassemia deletion type	Is a	Congenital anemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Alpha plus thalassemia deletion type	Interprets	Red blood cell count	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
4637143017	Alpha plus thalassaemia deletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4637144011	Alpha plus thalassemia deletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4637145012	Alpha plus thalassemia deletion type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
143020018	alpha^+^ Thalassemia, deletion type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
506995019	alpha^+^ Thalassaemia, deletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
506995019	alpha^+^ Thalassaemia, deletion type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
828465018	alpha^+^ Thalassemia, deletion type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
828465018	alpha^+^ Thalassemia, deletion type (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4637143017	Alpha plus thalassaemia deletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4637144011	Alpha plus thalassemia deletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4637145012	Alpha plus thalassemia deletion type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5980481000241110	thalassémie de type alpha plus par délétion	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5980491000241112	alpha-plus-thalassémie par délétion	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5980481000241110	thalassémie de type alpha plus par délétion	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5980491000241112	alpha-plus-thalassémie par délétion	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module