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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
831282019 Hereditary elliptocytosis due to alpha spectrin defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
15623011 Hereditary elliptocytosis due to alpha spectrin defect en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
15623011 Hereditary elliptocytosis due to alpha spectrin defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
831282019 Hereditary elliptocytosis due to alpha spectrin defect (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
831282019 Hereditary elliptocytosis due to alpha spectrin defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6238691000241118 EH (elliptocytose héréditaire) due à une anomalie de la spectrine alpha fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6238711000241116 elliptocytose héréditaire due à une anomalie de la spectrine alpha fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6238691000241118 EH (elliptocytose héréditaire) due à une anomalie de la spectrine alpha fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6238711000241116 elliptocytose héréditaire due à une anomalie de la spectrine alpha fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 haematologic sysem false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Is a Anaemia due to intrinsic red cell abnormality true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Is a Hereditary elliptocytosis true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to alpha spectrin defect Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary elliptocytosis due to alpha spectrin defect Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary elliptocytosis due to alpha spectrin defect Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary elliptocytosis due to alpha spectrin defect Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary elliptocytosis due to alpha spectrin defect Has interpretation Present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to alpha spectrin defect Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to alpha spectrin defect Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to alpha spectrin defect Associated morphology Elliptocyte (cell) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to alpha spectrin defect Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to alpha spectrin defect Interprets Haemolysis true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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