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15121005: Hereditary elliptocytosis due to glycophorin C deficiency (disorder)


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
25675015 Hereditary elliptocytosis due to glycophorin C deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
741824010 Hereditary elliptocytosis due to glycophorin C deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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