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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


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 hematologic system false Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Is a Hereditary elliptocytosis true Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Is a Anaemia due to intrinsic red cell abnormality true Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Hematopoietic system structure false Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets Spectrin false Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Erythrocyte false Inferred relationship Some 3
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Hematopoietic system structure false Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Has definitional manifestation Erythropenia false Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Body system structure false Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association Has interpretation Below reference range true Inferred relationship Some 1
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 1
Hereditary elliptocytosis due to beta spectrin defect in self-association Has interpretation Below reference range true Inferred relationship Some 2
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets Red blood cell count true Inferred relationship Some 2
Hereditary elliptocytosis due to beta spectrin defect in self-association Has interpretation Present true Inferred relationship Some 3
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets Hemolysis (observable entity) true Inferred relationship Some 3
Hereditary elliptocytosis due to beta spectrin defect in self-association Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site Erythrocyte true Inferred relationship Some 4
Hereditary elliptocytosis due to beta spectrin defect in self-association Associated morphology Elliptocyte true Inferred relationship Some 4
Hereditary elliptocytosis due to beta spectrin defect in self-association Occurrence Congenital true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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