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54006005: Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (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
3793710015 Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3793711016 Hereditary persistence of fetal hemoglobin delta beta plus thalassemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3793712011 Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3793714012 Hereditary persistence of foetal haemoglobin delta beta plus thalassaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3793721012 HPFH (hereditary persistence of fetal hemoglobin) delta beta plus thalassemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3793726019 HPFH (hereditary persistence of fetal haemoglobin) delta beta plus thalassaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3793727011 HPFH (hereditary persistence of foetal haemoglobin) delta beta plus thalassaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) est défini par la manifestation de (attribut) Erythropenia false Inferred relationship Some
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) est un(e) (attribut) Delta beta zero thalassemia true Inferred relationship Some
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) est un(e) (attribut) Hereditary persistence of fetal hemoglobin thalassemia true Inferred relationship Some
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) a pour interprétation (attribut) au-dessous de l'étendue de référence false Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) interprète (attribut) Measurement of total haemoglobin concentration false Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) interprète (attribut) Red blood cell count false Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) survenue (attribut) congénital true Inferred relationship Some 3
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 3
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder) localisation d'une constatation (attribut) Erythrocyte 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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