FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

61395005: Hereditary persistence of fetal hemoglobin G gamma 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
3793694018 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3793695017 Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3793698015 Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3800043011 HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3800044017 HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3800045016 HPFH (hereditary persistence of foetal haemoglobin) G gamma 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 G gamma beta plus thalassemia interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia est défini par la manifestation de (attribut) Erythropenia false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia est un(e) (attribut) Hereditary persistence of fetal hemoglobin thalassemia true Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia est un(e) (attribut) Beta plus thalassemia true Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia a pour interprétation (attribut) au-dessous de l'étendue de référence false Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia interprète (attribut) Measurement of total haemoglobin concentration false Inferred relationship Some 1
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia interprète (attribut) Red blood cell count false Inferred relationship Some 2
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia survenue (attribut) congénital true Inferred relationship Some 3
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 3
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia localisation d'une constatation (attribut) Erythrocyte false Inferred relationship Some
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia 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)

Back to Start