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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary elliptocytosis due to alpha spectrin defect a pour interprétation (attribut) présent (valeur de l'attribut) true Inferred relationship Some 3
Hereditary elliptocytosis due to alpha spectrin defect survenue (attribut) congénital true Inferred relationship Some 4
Hereditary elliptocytosis due to alpha spectrin defect localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 4
Hereditary elliptocytosis due to alpha spectrin defect morphologie associée (attribut) Elliptocyte (cell) true Inferred relationship Some 4
Hereditary elliptocytosis due to alpha spectrin defect Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Hereditary elliptocytosis due to alpha spectrin defect interprète (attribut) Hemolysis (observable entity) true Inferred relationship Some 3
Hereditary elliptocytosis due to alpha spectrin defect localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect est défini par la manifestation de (attribut) Erythropenia false Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect est un(e) (attribut) Hereditary disorder of hematologic system false Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect est un(e) (attribut) anémie causée par une anomalie constitutionnelle des érythrocytes true Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect est un(e) (attribut) Hereditary elliptocytosis true Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 1
Hereditary elliptocytosis due to alpha spectrin defect interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 1
Hereditary elliptocytosis due to alpha spectrin defect a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
Hereditary elliptocytosis due to alpha spectrin defect interprète (attribut) Red blood cell count true Inferred relationship Some 2
Hereditary elliptocytosis due to alpha spectrin defect localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect localisation d'une constatation (attribut) Erythrocyte false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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