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5994005: Hereditary elliptocytosis due to deficiency of 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
10964018 Hereditary elliptocytosis due to deficiency of protein 4.1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
798838013 Hereditary elliptocytosis due to deficiency of 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 deficiency of protein 4.1 a pour interprétation (attribut) présent (valeur de l'attribut) true Inferred relationship Some 3
Hereditary elliptocytosis due to deficiency of protein 4.1 interprète (attribut) Hemolysis (observable entity) true Inferred relationship Some 3
Hereditary elliptocytosis due to deficiency of protein 4.1 survenue (attribut) congénital true Inferred relationship Some 4
Hereditary elliptocytosis due to deficiency of protein 4.1 localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 4
Hereditary elliptocytosis due to deficiency of protein 4.1 Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Hereditary elliptocytosis due to deficiency of protein 4.1 morphologie associée (attribut) Elliptocyte (cell) true Inferred relationship Some 4
Hereditary elliptocytosis due to deficiency of protein 4.1 est défini par la manifestation de (attribut) Erythropenia false Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 est un(e) (attribut) Hereditary disorder of hematologic system false Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 est un(e) (attribut) Hereditary elliptocytosis true Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 est un(e) (attribut) anémie causée par une anomalie constitutionnelle des érythrocytes true Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 1
Hereditary elliptocytosis due to deficiency of protein 4.1 interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 1
Hereditary elliptocytosis due to deficiency of protein 4.1 a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
Hereditary elliptocytosis due to deficiency of protein 4.1 interprète (attribut) Red blood cell count true Inferred relationship Some 2
Hereditary elliptocytosis due to deficiency of protein 4.1 localisation d'une constatation (attribut) Erythrocyte false Inferred relationship Some 3
Hereditary elliptocytosis due to deficiency of protein 4.1 localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some

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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