25266006: Hereditary spherocytosis due to spectrin deficiency (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 hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\Anaemia\Anaemia due to intrinsic red cell abnormality\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\Anaemia\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\Anaemia\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\Hemolytic disorder (disorder)\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\Hemolytic disorder (disorder)\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Red blood cell destruction finding\Hemolysis\Hemolytic disorder (disorder)\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Finding of blood, lymphatics and immune system\Red blood cell destruction finding\Hemolysis\Hemolytic disorder (disorder)\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)

\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)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\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\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\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\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Cytopenia\Red blood cell count below reference range\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Measurement finding\Measurement finding outside reference range\Blood cell count outside reference range\Cytopenia\Red blood cell count below reference range\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin below reference range (finding)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Cytopenia\Red blood cell count below reference range\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Cytopenia\Red blood cell count below reference range\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\Red blood cell count below reference range\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Measurement finding\Red blood cell count - finding\Red blood cell count outside reference range\Red blood cell count below reference range\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)

\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)

\Functional finding\Red blood cell destruction finding\Hemolysis\Hemolytic disorder (disorder)\Hemolytic anemia\...

\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)

\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to intrinsic red cell abnormality\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of cellular component of blood\Anaemia\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of cellular component of blood\Anaemia\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of cellular component of blood\Hemolytic disorder (disorder)\Hemolytic anemia\Anemia due to membrane defect (disorder)\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of cellular component of blood\Hemolytic disorder (disorder)\Hemolytic anemia\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemolytic anemia\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Erythrocyte membrane abnormality\Hereditary spherocytosis (disorder)\Hereditary spherocytosis due to spectrin deficiency (disorder)

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
Hereditary spherocytosis due to spectrin deficiency (disorder)	Is a	Hereditary spherocytosis (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Defect	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to spectrin deficiency (disorder)	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to spectrin deficiency (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocytosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Has definitional manifestation	érythropénie	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary spherocytosis due to spectrin deficiency (disorder)	Is a	Disorder of hematopoietic structure (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to spectrin deficiency (disorder)	Has definitional manifestation	Hemolysis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary spherocytosis due to spectrin deficiency (disorder)	Associated morphology	Spherocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Finding site	Hematopoietic system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary spherocytosis due to spectrin deficiency (disorder)	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary spherocytosis due to spectrin deficiency (disorder)	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary spherocytosis due to spectrin deficiency (disorder)	Interprets	Red blood cell count	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary spherocytosis due to spectrin deficiency (disorder)	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary spherocytosis due to spectrin deficiency (disorder)	Interprets	Erythrocyte destruction	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to spectrin deficiency (disorder)	Has interpretation	Present (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Hereditary spherocytosis due to spectrin deficiency (disorder)	Interprets	Haemolysis	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Mild hereditary spherocytosis due to spectrin deficiency	Is a	True	Hereditary spherocytosis due to spectrin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin	Is a	True	Hereditary spherocytosis due to spectrin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Severe hereditary spherocytosis due to spectrin deficiency (disorder)	Is a	True	Hereditary spherocytosis due to spectrin deficiency (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
42354018	Hereditary spherocytosis due to spectrin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
755563011	Hereditary spherocytosis due to spectrin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
42354018	Hereditary spherocytosis due to spectrin deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
42354018	Hereditary spherocytosis due to spectrin deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
755563011	Hereditary spherocytosis due to spectrin deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
755563011	Hereditary spherocytosis due to spectrin deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6239241000241117	sphérocytose héréditaire due à un déficit en spectrine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6239241000241117	sphérocytose héréditaire due à un déficit en spectrine	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module