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73073009: Hereditary elliptocytosis due to beta spectrin defect in self-association (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
121372015 Hereditary elliptocytosis due to beta spectrin defect in self-association en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
813421012 Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
121372015 Hereditary elliptocytosis due to beta spectrin defect in self-association en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
121372015 Hereditary elliptocytosis due to beta spectrin defect in self-association en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
813421012 Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
813421012 Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6290451000241118 elliptocytose héréditaire due à un défaut d'autoassociation de la spectrine bêta fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6290461000241115 EH (elliptocytose héréditaire) due à un défaut d'autoassociation de la spectrine bêta fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6290451000241118 elliptocytose héréditaire due à un défaut d'autoassociation de la spectrine bêta fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6290461000241115 EH (elliptocytose héréditaire) due à un défaut d'autoassociation de la spectrine bêta fr Synonym (core metadata concept) Active Entire term case sensitive (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 beta spectrin defect in self-association Is a Hereditary disorder of haematologic sysem false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Is a Hereditary elliptocytosis true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Is a Anaemia due to intrinsic red cell abnormality true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets Spectrin false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Erythrocyte false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary elliptocytosis due to beta spectrin defect in self-association Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary elliptocytosis due to beta spectrin defect in self-association Has interpretation Present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets Haemolysis true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary elliptocytosis due to beta spectrin defect in self-association Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to beta spectrin defect in self-association Associated morphology Elliptocyte (cell) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to beta spectrin defect in self-association Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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