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75443009: Hereditary elliptocytosis due to abnormal protein 4.1 (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
125306014 Hereditary elliptocytosis due to abnormal protein 4.1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
816053017 Hereditary elliptocytosis due to abnormal protein 4.1 (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 abnormal protein 4.1 interprète (attribut) Hemolysis (observable entity) true Inferred relationship Some 3
Hereditary elliptocytosis due to abnormal protein 4.1 survenue (attribut) congénital true Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 morphologie associée (attribut) Elliptocyte (cell) true Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 a pour interprétation (attribut) présent (valeur de l'attribut) true Inferred relationship Some 3
Hereditary elliptocytosis due to abnormal protein 4.1 localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 est défini par la manifestation de (attribut) Erythropenia false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 est un(e) (attribut) anémie causée par une anomalie constitutionnelle des érythrocytes true Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 est un(e) (attribut) Hereditary elliptocytosis true Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 est un(e) (attribut) Hereditary disorder of hematologic system false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 1
Hereditary elliptocytosis due to abnormal protein 4.1 interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 1
Hereditary elliptocytosis due to abnormal protein 4.1 a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
Hereditary elliptocytosis due to abnormal protein 4.1 interprète (attribut) Red blood cell count true Inferred relationship Some 2
Hereditary elliptocytosis due to abnormal protein 4.1 localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 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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