73073009: Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder)

\Congenital hemolytic anemia\Hereditary elliptocytosis\Hereditary elliptocytosis due to beta spectrin defect in self-association

\Hereditary hemolytic anemia\Hereditary elliptocytosis\Hereditary elliptocytosis due to beta spectrin defect in self-association

Descriptions:

Id Description Lang Type Status Case? Module

121372015 Hereditary elliptocytosis due to beta spectrin defect in self-association en Synonym Active Entire term case insensitive SNOMED CT core module

813421012 Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary elliptocytosis due to beta spectrin defect in self-association	Is a	Hereditary disorder of hematologic system	false	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Is a	Hereditary elliptocytosis	true	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Is a	Anemia due to intrinsic red cell abnormality	true	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Interprets	Spectrin	false	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier	3
Hereditary elliptocytosis due to beta spectrin defect in self-association	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	1
Hereditary elliptocytosis due to beta spectrin defect in self-association	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	1
Hereditary elliptocytosis due to beta spectrin defect in self-association	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Hereditary elliptocytosis due to beta spectrin defect in self-association	Interprets	Red blood cell count	true	Inferred relationship	Existential restriction modifier	2
Hereditary elliptocytosis due to beta spectrin defect in self-association	Has interpretation	Present	true	Inferred relationship	Existential restriction modifier	3
Hereditary elliptocytosis due to beta spectrin defect in self-association	Interprets	Hemolysis	true	Inferred relationship	Existential restriction modifier	3
Hereditary elliptocytosis due to beta spectrin defect in self-association	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	4
Hereditary elliptocytosis due to beta spectrin defect in self-association	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	4
Hereditary elliptocytosis due to beta spectrin defect in self-association	Associated morphology	Elliptocyte	true	Inferred relationship	Existential restriction modifier	4
Hereditary elliptocytosis due to beta spectrin defect in self-association	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	4

Inbound Relationships

Characteristic

Refinability

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
121372015	Hereditary elliptocytosis due to beta spectrin defect in self-association	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
813421012	Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module