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8857001: Hereditary elliptocytosis due to alpha spectrin defect (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
15623011 Hereditary elliptocytosis due to alpha spectrin defect en Synonym Active Entire term case insensitive SNOMED CT core module
831282019 Hereditary elliptocytosis due to alpha spectrin defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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