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8857001: Hereditary elliptocytosis due to alpha spectrin defect (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
15623011 Hereditary elliptocytosis due to alpha spectrin defect en Synonym Active Case insensitive SNOMED CT core
831282019 Hereditary elliptocytosis due to alpha spectrin defect (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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